Founded in 2012, Planet Pharma is a global leader in life sciences recruitment and staffing, specializing in Pharmaceuticals, Biotechnology, Medical Device, Labs & Healthcare, Specialty Providers, CMOs / CDMOs, and Contract Research Organizations (CROs). We provide the following solutions: Contract & Direct Hire (Permanent) Staffing, Strategic Resourcing, Retained & Executive Search, Functional Service Provider (FSP), and Global Workforce Solutions.

Planet Pharma has offices throughout North America, Europe, and APAC. All locations operate with shared attributes at the heart of everything we do!

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Industry: Staffing and Recruiting
Company Size: 1,001-5,000 employees

Planet Pharma

Savvy Admin PROD

Target PR Range: 38-48/hr

- Depending on experience

The ideal candidate is expected to demonstrate working knowledge and understanding of formulation and manufacturing process development for sterile liquid drug products, including solutions, emulsions, and suspensions. Knowledge of polymer sciences is highly desired. Experience with various sterilization techniques for liquid drug products, such as filtration, and autoclaving, is desired. The candidate should have experience with analytical measurements and characterization techniques such as pH, osmolality, viscosity/rheology, turbidity, particle size, and physical appearance. Hands-on experience with HPLC and UPLC (with detectors such as UV, PDA, and RI) is also desired but not required.

**Key Responsibilities**

Th essential responsibilities of this position include:

- Conducting laboratory experiments for development of pharmaceutical products, with focus on sterile liquid dosage forms under supervision and guidance of the group members.

- Conducting analytical & characterization experiments to generate scientifically sound data supporting the formulation and manufacturing process development efforts of liquid dosage forms.

- Designing and interpreting experiments independently whenever the situation demands.

- Employing problem-solving and creative scientific skills.

- Working independently to generate accurate, reliable data on time and accurately documenting in electronic laboratory notebooks.

- Practicing good communication (oral and written) and interpersonal skills.

Upon assignment given by the team, the candidate will independently plan and execute lab-scale experiments related to sterile liquid formulation and manufacturing process development. Prompt and accurate documentation of experiments, results, and conclusions to ensure data integrity and accuracy is critical. The candidate independently analyzes and interprets technical data and utilizes statistical techniques as needed.

Additional responsibilities include proper maintenance of laboratory equipment and instrumentation to ensure laboratory operational capability.

**Minimum Requirements For Education And Experience**

This position requires a bachelor’s degree in chemistry, chemical engineering, pharmacy, or other relevant scientific discipline with 3-5 years of relevant industry experience or a master’s degree in chemistry, chemical engineering, pharmacy or other relevant scientific discipline with 2 years of relevant industry experience.

Strong technical writing and communication skills. Must be proficient using Word, Excel, and statistical software. Knowledge of fundamental application of statistics is preferred.

Experience in analyzing data and writing technical reports is desired.

Scientist II

**Scientist II **

**Location: ** Irvine, CA (on‑site)

**Contract: ** 12 months

**Pay Rate: ** Target $45–46/hr

**Position Overview **

We are seeking a Formulation Scientist to support the development of sterile liquid pharmaceutical drug products. The ideal candidate will have hands‑on experience with liquid dosage form formulation and process development, strong laboratory execution skills, and the ability to independently generate and interpret scientifically sound data.

This role focuses on solutions, emulsions, and suspensions, with exposure to polymer science, sterilization techniques, and analytical characterization methods.

**Key Responsibilities **

- Conduct laboratory experiments supporting the development of sterile liquid dosage forms under general supervision.

- Execute analytical and characterization testing to support formulation and manufacturing process development.

- Independently design, plan, and interpret experiments as needed.

- Utilize problem‑solving and scientific reasoning to address formulation and process challenges.

- Accurately document experiments, results, and conclusions in electronic laboratory notebooks (ELN).

- Analyze and interpret technical data using fundamental statistical tools when appropriate.

- Prepare clear and concise technical summaries and reports.

- Maintain laboratory equipment and instrumentation to ensure operational readiness.

- Collaborate effectively with cross‑functional team members and communicate results clearly (written and verbal).

**Required Skills & Experience **

- Working knowledge of formulation and manufacturing process development for sterile liquid drug products, including solutions, emulsions, and suspensions.

- Experience with analytical and characterization techniques, such as:

- pH

- Osmolality

- Viscosity / Rheology

- Turbidity

- Particle size

- Physical appearance evaluations

- Knowledge of polymer sciences (highly desired).

- Familiarity with sterilization techniques for liquid drug products (e.g., filtration, autoclaving).

- Strong technical writing, documentation, and data analysis skills.

- Proficiency with Microsoft Word, Excel, and statistical software.

**Nice to Have: **

- Hands‑on experience with HPLC or UPLC (UV, PDA, RI detectors).

**Education & Qualifications **

- Bachelor’s degree in Chemistry, Chemical Engineering, Pharmacy, or related scientific discipline

- plus 3–5 years of relevant industry experience

- OR

- Master’s degree in a similar discipline

- plus 2 years of relevant industry experience

Scientist

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuroscience, eye care, aesthetics and other areas of unmet need.  

Learn more about us at www.abbvie.com and review our community guidelines at https://www.abbvie.com/social-media-community-guidelines.html.

Industry: Pharmaceutical Manufacturing
Company Size: 10,001+ employees

AbbVie

**Company Description**

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

**Job Description**

The Toxins group within the Product Development, Science & Technology (PDS&T) - Biologics organization supports manufacturing, process validation, regulatory submission, and continuous improvement for late-stage and commercial manufacturing of biological toxin products at AbbVie. We have an exciting opportunity for a Scientist I position based in Irvine, CA. This role involves leveraging scientific and bioengineering principles to develop bioassays for analytical testing at drug substance and drug product release and stability time points. The candidate must possess in-depth knowledge and hands-on experience in a range of techniques, including but not limited to molecular cloning, mammalian cell culture, PCR, Western blot, protein expression, purification, bioassay, transfection, and laboratory automation platforms. Moreover, excellent communication skills and the ability to thrive in a multi-disciplinary and cross-functional team environment are essential for success in this role.

**Key responsibilities include:**

- Develop, program, operate, and troubleshoot robotic automation platforms, including Hamilton STAR liquid handlers and Opentrons, to support high-throughput screening and testing.

- Lead scientific initiatives by generating innovative technical ideas and strategic approaches to advance research goals and address experimental challenges.

- Demonstrate strong scientific judgment by aligning research activities with project objectives and adapting experimental plans based on new data, evolving priorities, and project developments.

- Design, execute, and interpret complex experiments using rigorous, reproducible methodologies. Develop, optimize, and implement novel experimental protocols by leveraging emerging technologies to advance scientific progress and resolve technical issues.

- Maintain current expertise in relevant scientific and technical disciplines and apply best practices from current literature to experimental design, troubleshooting, and method development.

- Establish and manage experimental timelines, track progress closely, and ensure timely delivery of project milestones through strong organization and time-management.

- Draft, review, and edit SOPs, technical reports, publications, presentations, and patent applications in accordance with industry and regulatory standards.

- Communicate scientific concepts, experimental data, and key findings effectively to cross-functional teams and stakeholders through clear written and oral presentations.

**Qualifications**

- Bachelor’s degree, or equivalent education, with typically 5 years of relevant experience; or Master’s degree, or equivalent education, with typically 2 years of relevant experience in Cell and Molecular Biology, Biochemistry, Biochemical or Biomedical Engineering, Biotechnology, or a closely related discipline.

- Hands-on experience with scripting and programming robotic liquid handlers (e.g., Hamilton STAR and Opentrons) and proficiency in software platforms like VENUS and Python.

- Experience translating manual cell-based assays, including ELISA and potency assays, into automated workflows.

- Practical experience with molecular cloning, mammalian cell culture, PCR, Western blotting, bioassays, and transfection procedures.

- Knowledgeable in genome editing approaches, including CRISPR/Cas9, with a solid understanding of experimental design, execution, and validation of gene-editing studies.

- Experience in optimizing and qualifying cell-based potency assays, including sample testing.

- Strong computer skills essential for scientific research, including word processing, spreadsheets, presentation software, and advanced data analysis. Ability to analyze, interpret, and present complex datasets using scientific software such as Python, R, and JMP.

- Previous GxP experience and attention to detail in documentation preferred.

- Demonstrated ability to design experiments, solve problems creatively, develop comprehensive experimental plans, and independently troubleshoot and validate results.

- Ability to stay current with scientific advances, critically evaluate relevant literature, and rapidly incorporate new concepts and techniques into research activities.

- Detail-oriented, with a proven ability to generate high-quality, reproducible data within tight deadlines.

- Strong interpersonal and collaboration skills, with the ability to work effectively in multidisciplinary, cross-functional teams and communicate complex scientific concepts clearly in both verbal and written formats.

- Self-motivated, adaptable, and committed to scientific discovery, continuous learning, and process improvement.

- Experience developing and optimizing these models for research or drug discovery applications is highly desirable.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.

- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.

- This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Scientist I

Sustainability is our business.  

As the world’s largest specialist sustainability consultancy, ERM partners with clients to operationalize sustainability at pace and scale, deploying a unique combination of strategic transformation and technical delivery capabilities. This approach helps clients to accelerate the integration of sustainability at every level of their business.  

With more than 50 years of experience, ERM’s diverse team of 8000+ experts in 40 countries and territories helps clients create innovative solutions to their sustainability challenges, unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.

Industry: Business Consulting and Services
Company Size: 5,001-10,000 employees

**Environmental Resources Management, Inc. (ERM) **is seeking a motivated **Principal Consultant, Air Quality - Engineering / Scientist **to join the**ERM **team in**Irvine, CA **or **Denver, CO. ** This is a partner-track opportunity for an air quality professional looking to further advance their career with a global environmental leader and to make a significant impact in successfully implementing ERM's global strategy.

ERM’s Air Quality Service Area is a recognized leader in the marketplace. Our technical community pursues and wins highly innovative engagements for the most interesting clients, providing the full breadth of air quality and climate change services. With annual global sales in excess of $50 million, ERM’s Air Quality Service Area is one of the largest among its peers in our industry and is steadily growing at a double-digit pace. In North America alone, ERM has more than 300 dedicated air quality professionals assisting clients with projects as diverse as developing strategic approaches at the corporate level to upcoming regulatory drivers, to leading complex capital projects through the many hurdles associated with the New Source Review (NSR) permitting program.

ERM is structured to encourage collaboration and networking among regional offices, providing opportunities to collaborate with ERM’s national air quality technical team to share expertise and consulting opportunities. Our leaders proactively work together to build strategies and campaigns around key business drivers for our clients, with the primary focus of finding and delivering high-profile rewarding projects and building our business, whether it be for permitting compliance strategy and emission inventories, greenhouse gas reporting regulations, new air dispersion modeling challenges, new California and federal rule standards, energy management and transition, or climate change adaptation.

As a senior leader on this team, you will be fully accountable for successfully selling and consulting for air quality and compliance projects to build a sustainable business locally, while networking with ERM's global Air Quality Technical Team to share best practices across the industry. The ideal candidate will be well connected in the regulatory and air permitting community and have established relationships with manufacturing, technology, oil & gas, and/or chemical companies to expand our corporate and facility-level compliance services in the sector of the candidate’s expertise in California and the Southwest.

**Responsibilities**

- Contribute to the development and implementation of a strategic market/business plan, provide leadership, and deliver financial results to expand ERM's Air Quality Service Area and client base, particularly in the manufacturing, technology, oil & gas, and/or chemical sectors. Serve as a key member of the “core” technical team to drive double-digit profitable growth of ERM’s air quality services across North America.

- Serve as a Senior expert for strategic air permits and compliance programs for a variety of industrial clients with complex technical/regulatory issues.

- Work closely with clients and develop strong relationships to understand specific processes and develop a permitting and compliance strategy to help clients maintain maximum operating flexibility. Achieve client’s expectations for scope, budget, schedule, and quality.

- Manage project deliverables, budgets, and schedules as a lead for our existing teams.

- As a “seller/doer,” contribute to expanding ERM’s air consulting and compliance services annually. Identify and develop new opportunities, prepare effective technical proposals, and take an active leadership role in the development of new business with new and existing clients. Develop and expand client relationships that generate repeat business.

- Capitalize on existing client relationships to expand ERM’s profile and market share in the regional air quality market and other service-line offerings through a combination of excellence in technical delivery and business development.

- Mentor junior and mid-level staff in the proper planning and execution of air quality projects, and in directing or conducting independent technical reviews of work products.

- Support the general growth and development of ERM’s Global Air Quality Services.

- Collaborate with other ERM global practitioners to execute air quality projects, including participating on teams comprised of air quality professionals from multiple offices around the global organization.

- Develop a working understanding of ERM’s other consulting service areas and actively support cross selling these services to existing clients.

**Requirements**

- Bachelors in chemical, environmental engineering, mechanical engineering, environmental science or related degree. Or equivalent experience.

- 6+ years of relevant experience.

- Experience and knowledge of local, state, and federal air regulations.

- Ability to lead and grow the business in a dynamic market environment.

- Advanced expertise in air permitting and climate change.

- Strong track record of managing project deliverables, schedule, and budgets.

- In-depth understanding of the manufacturing, oil & gas, technology, and chemical industries in California and the companies operating in this sector, including existing relationships that can be leveraged into new business.

- Consistent "seller/doer" track record, including successfully winning large and strategic projects.

- An established reputation in the local marketplace and recognized technical expertise in one of ERM’s existing service offerings, which include, but are not limited to air quality and climate change, environmental, health, and safety compliance assurance, process safety, sustainability, and environmental permitting.

- Ability to build, coach, and mentor collaborative teams.

- Excellent communication (written/verbal), strategic thinking, negotiation, presentation, and “people” skills.

- Positive outlook, collaborative, and driven by the success of ERM as a global company.

**Preferred**

- 8+ years experience of solid air quality consulting experience, with a high degree of technical competence in Title V, PSD, NSR, BACT, and MACT.

- Certification in field: P.E., CSP, CHMM, or similar registration.

- Familiarity with stack testing and ambient air measurements.

- Advanced expertise in other environmental compliance-related areas for example: air dispersion modeling, stormwater, Spill Preventions, Control, and Countermeasure Plans, waste, water resources, Risk Management Planning, California Environmental Quality Act permitting, multi-media auditing, etc.

~~For the **Principal Consultant, Air Quality - Engineering / Scientist **position, we anticipate the annual base pay of **$122,612- $166,230 USD. ** An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. **We also may have instances where compensation may be outside of the range, based on the factors noted above **. This job is also eligible for an annual discretionary based performance bonus.~~

~~We offer a comprehensive package of benefits including paid time off, paid parental leave, medical, dental, vision, life, disability and AD&D insurance, 401(k) or RRSP/DPS P, and any other benefits to eligible employees as applicable.~~

~~You can apply for this role through https://www.erm.com/careers/apply/ or through the internal careers portal if you are a current employee.~~

~~Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, or any other form of compensation that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.~~

**Who We Are**

As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.

At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career. We also see our diversity as a strength that helps us create better solutions for our clients. Our diverse team of world-class experts supports clients across the breadth of their organizations to operationalize sustainability, underpinned by our deep technical expertise in addressing their environmental, health, safety, risk and social issues. We call this capability our “boots to boardroom” approach for its comprehensive service model that allows ERM to develop strategic and technical solutions that advance objectives on the ground or at the executive level.

Please submit your resume and brief cover letter.

ERM does not accept recruiting agency resumes. Please do not forward resumes to our jobs alias, ERM employees or any other company location. ERM is not responsible for any fees related to unsolicited resumes.

ERM is proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, gender, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Thank you for your interest in ERM!

Principal Consultant, Air Quality - Engineering / Scientist

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