Sarepta Therapeutics

Quality Control Analyst (Sun-Wed shift)

Sarepta Therapeutics$78K — $98K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • B.S. in biology or biochemistry, focusing on molecular biology, cell biology, or virology
  • 2-5 years of relevant experience, ideally with gene therapy products
  • Strong understanding of method development using capillary-based western blotting
  • Experience in cGMP environments is preferred
  • In-depth knowledge of cell culture methods and associated assays
  • Demonstrated organizational skills in laboratory settings
  • Effective communication skills, both written and verbal

Responsibilities

  • Perform potency assays for lot release and stability testing from Sunday to Wednesday
  • Support troubleshooting and optimization of cell culture and bioassays
  • Prepare, qualify, and release standards for in-vitro potency methods
  • Test new cell lines for potential use in potency assays
  • Maintain cell banks with cryogenic storage practices
  • Assist in method development, transfer, and validation for gene therapy products
  • Document and maintain clear lab records for compliance purposes

Benefits

  • Health, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off and holidays
  • Continuing education opportunities
  • Work in a collaborative and innovative environment
Full Job Description

The Importance of the Role

The successful candidate will work within the QC team, testing gene therapy products utilizing cell-based assays (Potency assay) in support of clinical and commercial lot release and stability activities. These assays are conducted in-house at the Sarepta facility in Andover, MA., with additional testing performed at contract testing laboratories (which may require periodic SME support). The successful candidate will have hands-on experience with cell-based in-vitro potency assays, cell culture, SDS-PAGE, western blot, Automated Western blot assays, enzyme activity measurements, protein extraction, purification, and quantification methods. The required work involves handling and testing samples in a BSL-2 environment. All aspects of this position involve working in a GMP-compliant manner. The successful candidate will also assist in authoring and managing quality events (deviations, CAPAs, Change Controls etc.), as well as conducting data analysis and trending (for internal and external testing laboratories). Upon successful completion of training, this position will be fully onsite comprising 4 -10-hour days per week: Sunday-Wednesday shift. Work will also include coverage for holidays that fall during the shift schedule.

The Opportunity to Make a Difference

Responsibilities & Duties:
•    Performing potency assay for lot release and stability testing carried out Sunday-Wednesday. 
•    Support maintenance, troubleshooting and optimization of cell culture and bioassays such as in-vitro potency.
•    Prepare, qualify, and release standards for the in-vitro potency methods.
•    Test new cell lines for use in new potency assays
•    Maintaining cell banks on cryogenic storage
•    Support method development, transfer and qualification/validation activities associated with the cell-based potency assays for AAV-based gene therapy products and other assays as required.
•    Create and maintain clear and concise lab records and documentation.
•    Support the authoring of test methods, development reports, study protocols, and validation reports.


•    Support sample management: Inventory and tracking of incoming and outgoing samples.
•    Collaborate with team leads and managers to optimize a smooth workflow for efficient management of team activities.
•    Perform other related duties incidental to the work described.

Qualifications & Skills:
•    B.S. degree in biology or biochemistry with course work emphasizing molecular biology, cell biology, and/or virology. 2-5 years of relevant experience is necessary. Experience working with gene therapy products is highly desired.
•    A strong understanding of method development and routine testing operations using capillary based western blotting system is desired.
•    Experience working in a cGMP environment is desired.
•    A strong understanding of cell culture methods - Potency, Agarose gel electrophoresis, Western blot, SDS-PAGE, and cell culture is necessary.
•    Experience in general laboratory organization, experimental design, and documentation (GDP) with adherence to cGMP is necessary.
•    Must be able to operate as a part of a team.
•    Attention to details is a must.
•    Effective written and verbal communication skills.
 

More about You

N/A

What Now?

We’re always looking for solution-oriented, critical thinkers.

So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply.
 

#LI-Onsite

This position requires work on site at one of Sarepta’s facilities in the United States.

The targeted salary range for this position is $78,400 - $98,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta’s compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity.

Candidates must be authorized to work in the U.S.

Sarepta Therapeutics offers a competitive compensation and benefit package.

About Sarepta Therapeutics

Sarepta Therapeutics, Inc. is an American biotechnology company focused on the discovery and development of RNA-targeted therapeutics. The company's lead product candidate is eteplirsen, a treatment for Duchenne muscular dystrophy (DMD). The company is also developing other RNA-targeted therapeutics for the treatment of other neuromuscular and infectious diseases. Sarepta Therapeutics was founded in 1980 as AntiVirals, Inc. and changed its name to AVI BioPharma, Inc. in 2000. The company changed its name to Sarepta Therapeutics, Inc. in 2012.
Learn more about Sarepta Therapeutics
Size
840 employees
Market Cap
$11.3 billion
Industry
Net Income
-$554.1 million
Founded
1980
5 Year Trend
+164.5%
Revenue
$540 million
NASDAQ

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