Avid Bioservices, Inc.

Sr. Research Associate, Analytical Development

Avid Bioservices, Inc.$84K — $105K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 4+ years industry experience in a QC or Analytical lab (BS degree) in Biochemistry, Chemistry, Biology, or pharmaceutical sciences
  • 2+ years industry experience in a QC or Analytical lab (MS degree)
  • Proficient in analytical testing and equipment utilizing analytical biochemistry methods
  • Skilled in writing reports, procedures, and specifications
  • Familiar with GMPs and regulatory audits
  • Experience in Potency/ELISA and/or HPLC is essential
  • Knowledge of protein characterization, electrophoresis, chromatography, and assay validation/qualification

Responsibilities

  • Perform and review routine wet chemistry assays, ELISA/cell-based immunoassays, electrophoresis (SDS-PAGE/IEF) and HPLC
  • Train and supervise junior analysts in experimental work
  • Develop, review, revise, and write test methods and standard operating procedures
  • Lead validation projects, investigations, and method development
  • Interface with Quality Control for cGMP testing methods
  • Support continuous improvement initiatives
  • Assist with regulatory inspections and other duties as assigned

Benefits

  • Comprehensive health, dental, and vision insurance
  • 401(k) matching program
  • Paid time off
  • Support for career growth and development
  • Inclusive work environment
Full Job Description
Your Role:

Are you an experienced Sr. Research Associate, Analytical Development looking to take the next step in your career? We're seeking a talented and passionate individual to join our Analytical Development team as we develop cutting-edge protein biologics. As our Sr. Research Associate, you'll have the opportunity to focus on developing Cell-based, ELISA, HPLC, CE, PCR and/or SDS-PAGE methods, and you'll work alongside experienced analytical scientists and process development scientists to identify and characterize protein biologics. This position offers the chance to interface with our Quality Control testing group as methods are transferred into that group for cGMP testing, and you may also have the opportunity to interface with external clients. Don't miss out on this exciting opportunity to join a team that's making a difference in the world of biologics. Apply now and take your career to the next level!

Key Responsibilities:
  • Perform and review routine wet chemistry assays and ELISA/cell-based immunoassays, electrophoresis (SDS-PAGE/IEF) and HPLC.
  • 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.
  • Knowledgeable of company cGMPs as well as industry regulations that apply to job functions. Participates in regulatory inspections.
  • Support continuous improvement initiatives.
  • Other duties as assigned.

Minimum Qualifications:
  • 4+ years industry experience working in a QC or Analytical lab (with a BS degree) preferably Biochemistry, Chemistry, Biology or pharmaceutical sciences
  • 2+ years industry experience working in a QC or Analytical lab (with a MS degree)
  • Analytical testing and equipment utilizing analytical biochemistry methods
  • Writing reports/procedures/specifications
  • GMPs and regulatory audits
  • Potency/ELISA and/or HPLC experience is essential.
  • Should also have experience with most if not all the following: protein characterization, electrophoresis, chromatography, and assay validation/qualification.

Preferred Qualifications:
  • Experience with Octet, liquid handler and Maurice is a plus!

Position Type/Expected Hours of Work:

This role is a full-time position operating Monday through Friday, unless otherwise stated by Supervisor. Any scientific staff member can expect to work overtime, including during the weekends. Off-site meetings with clients and regulatory agencies are a usual occurrence.

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.

About Avid Bioservices, Inc.

Avid Bioservices, Inc. is a contract development and manufacturing organization (CDMO) focused on development and CGMP manufacturing of biopharmaceutical drug substances derived from mammalian cell culture. The company provides a comprehensive range of process development, high quality CGMP clinical and commercial manufacturing services for the biotechnology and biopharmaceutical industries. With 25 years of experience producing monoclonal antibodies and recombinant proteins in batch, fed-batch and perfusion modes, Avid's services include CGMP clinical and commercial drug substance manufacturing, bulk packaging, release and stability testing and regulatory submissions support. The company also provides a variety of process development activities, including cell line development and optimization, cell culture and feed optimization, analytical methods development and product characterization.
Learn more about Avid Bioservices, Inc.
Size
321 employees
Market Cap
$873.5 million
Industry
Net Income
$4.4 million
5 Year Trend
+15.7%
Revenue
$80.8 million
NASDAQ

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