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Transforming the CDMO experience: Unrivaled expertise. Worldclass facilities. Exceptional quality. Personalized process.
The Role
Develops and performs analytical methods for protein biologics using ELISA, cell-based assays, HPLC, capillary electrophoresis, and electrophoresis. Supports validation, process development, stability studies, method transfers, investigations, and cGMP testing. Responsibilities include reviewing data, writing methods and procedures, conducting trending analysis, participating in regulatory inspections, leading analytical studies, training junior analysts, and supporting continuous improvement. The role interfaces with Quality Control, process development teams, and external clients in GMP and non-GMP environments.
Summary Generated by Built In
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
The Associate Scientist, Analytical Development will have the opportunity to focus on developing cell-based, ELISA, HPLC, and/or CE methods and will work alongside experienced analytical scientists and process development scientists to identify and characterize protein biologics. This position offers the chance to interface with Quality Control as methods are transferred into that group for cGMP testing, as well as to interface with external clients. The Associate Scientist will perform testing and sampling to support validation, process development, and stability studies in a non-GMP and GMP environment. They will have a substantial understanding of the job and apply knowledge and skills to complete a wide range of tasks, as well as support and lead continuous improvement initiatives.
Key Responsibilities:
Key Responsibilities:
- Perform and review routine wet chemistry/ELISA/cell-based immunoassays, electrophoresis (SDS-PAGE/CE) and/or HPLC.
- Must use scientific reasoning when making decisions regarding the quality of the data reported. Expected to research/gather information without supervision and to make scientifically sound decisions based on knowledge and experience.
- May train/supervise the experimental work of more junior analysts and may be a member of interdepartmental/tech transfer teams.
- Develop, review, revise and write test methods, standard operating procedures and may perform trending analysis. May be designated as study lead for validation projects, investigations, and method development projects.
- Previous experience in either HPLC, CE or Potency/ELISA assay methodologies is required.
- Knowledge of company cGMPs as well as industry regulations that apply to job functions. Participate in regulatory inspections.
- Support continuous improvement initiatives.
- Other tasks as assigned.
Minimum Qualifications:
- BS degree in Biochemistry, Chemistry, Biology or a related field is required.
- 5 + years of biotech industry experience working in a QC or analytical lab.
- Previous experience with analytical testing and equipment utilizing analytical biochemistry methods, writing reports/procedures/specifications, GMPs and regulatory audits required.
- HPLC, CE, or Potency/ELISA experience is essential.
- Should have also have experience with protein characterization, electrophoresis, chromatography, and assay validation/qualification.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $84,000 - $105,000 annually, depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
- You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
- Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
- You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
- You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.
Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.
Skills Required
- Bachelor’s degree in Biochemistry, Chemistry, Biology, or a related field
- 5 or more years of biotech industry experience in a quality control or analytical laboratory
- Experience with analytical testing equipment and analytical biochemistry methods
- Experience writing reports, procedures, and specifications
- Knowledge of GMPs and experience with regulatory audits
- Experience with HPLC, capillary electrophoresis, or potency/ELISA assay methodologies
- Experience with protein characterization, electrophoresis, chromatography, and assay validation or qualification
Avid Bioservices Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Avid Bioservices and has not been reviewed or approved by Avid Bioservices.
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Healthcare Strength — Health coverage includes medical, dental, and vision alongside life and disability insurance. Plan breadth is presented as solid, with health benefits frequently highlighted as a strong element of the package.
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Equity Value & Accessibility — An Employee Stock Purchase Plan with a discounted purchase feature and the availability of stock grants provide accessible ownership opportunities. These components add long-term value beyond base pay.
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Fair & Transparent Compensation — Pay ranges are posted for some roles, offering upfront clarity on expected compensation. This transparency supports clearer expectations during hiring.
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The Company
What We Do
Avid Bioservices is transforming the CDMO experience, with more than 30 years of unrivaled experience manufacturing biologics, and world-class mammalian protein facilities. We’ve produced more than 250 commercial batches, and 5 commercial products marketed in 90+ countries. For more than 10 years, we’ve maintained a flawless quality track record which we’re committed to uphold. We do it right the first time, which saves money and time. From early-stage to late-stage, concept to market, every part of our process is personalized. We’re your advocates, your trusted experts, your true partners.
