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Associate Generic Pharmaceutical Jobs (NOW HIRING)

Value Drug Company

Director of Sales

Duncansville, PA · On-site

Championing company programs that support customer success and increase generic pharmaceutical ... Associate degree or equivalent combination of education and extensive sales experience. * Strong ...

Value Drug Company

Director of Sales

Duncansville, PA · On-site

Championing company programs that support customer success and increase generic pharmaceutical ... Associate degree or equivalent combination of education and extensive sales experience. * Strong ...

TopRx

Be Seen First

Assistant Sales Manager

Memphis, TN · On-site

$63K - $68K/yr

... associate engagement. • Function as liaison between the account manager's questions and other ... Company Description A generic pharmaceutical distributor servicing pharmacies across the country ...

Cipla

QA Associate IT

Fall River, MA

$76K - $103K/yr

Job Title : QA Associate - IT FLSA Classification : Full-Time, Exempt Professional Work Location ... is a leading global pharmaceutical company, dedicated to high-quality, branded and generic ...

Cipla

QA Associate IT

Fall River, MA · On-site

$76K - $103K/yr

Job Title : QA Associate - IT FLSA Classification : Full-Time, Exempt Professional Work Location ... is a leading global pharmaceutical company, dedicated to high-quality, branded and generic ...

Astrix Inc

QC Associate Scientist

Concord, OH · On-site

We're hiring an Associate Scientist with analytical experience to join a global leader in the development and production of active pharmaceutical ingredients (APIs) for CDMO partners and generic ...

Adecco

Pharmacist

Clearwater, FL

$146K - $150K/yr

Makes decisions regarding generic substitution of prescribed pharmaceuticals * Makes outbound or ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Cipla

QA Associate IT - DPI

Hauppauge, NY · On-site

$76K - $103K/yr

Subsidiaries or Affiliates. Job Title: QA Associate (IT) Location: Hauppauge, NY (Onsite ... S. with both a generic and brand division. InvaGen Pharmaceuticals, Inc. InvaGen Pharmaceuticals is ...

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How much do associate generic pharmaceutical jobs pay per hour?

As of Jun 24, 2026, the average hourly pay for associate generic pharmaceutical in the United States is $26.86, according to ZipRecruiter salary data. Most workers in this role earn between $23.80 and $30.05 per hour, depending on experience, location, and employer.
What cities are hiring for Associate Generic Pharmaceutical jobs? Cities with the most Associate Generic Pharmaceutical job openings:
What are the most commonly searched types of Generic Pharmaceutical jobs? The most popular types of Generic Pharmaceutical jobs are:
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Associate Generic Pharmaceutical jobs near you
Infographic showing various Associate Generic Pharmaceutical job openings in the United States as of June 2026, with employment types broken down into 3% Full Time, and 97% Part Time. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $55,870 per year, or $26.9 per hour.

QC Lab Tech (Stability Coordinator) (Pharmaceutical Manufacturing)

Granules Pharmaceuticals

Chantilly, VA

$20.50 - $25.75/hr

Other

Posted 22 days ago

Job description

Description

Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!

With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.

Job Summary:

Perform a variety of activities to administer the stability program and manage data generated in support of the company's quality program. 

Essential Responsibilities:

  • Comply with the requirements of stability standard operating procedure.
  • Data entry and usage of stability software.
  • Review stability program annually and recommend revision when necessary.
  • Provide stability summary to QC Director upon completion of study.
  • Assures that stability samples are disposed of according to GMP guidelines.
  • Will assist in preparing and maintaining batch records, certificate of analysis, maintain/control and file records of raw material specification and finished product specification.
  • Responsible for ensuring stability chambers and monitoring system are performing within set requirements. 
  • Employee uses professional skills and concepts to solve a variety of often complex situations. Able to make clear and concise decisions of vast importance in limited period of time. Must be able to perform multiple tasks in the proper sequence to effectively reach desired goals.

Requirements:

  • Minimum Associate's Degree, Bachelor's degree preferred in pharmacy, chemistry or related scientific field
  • 0-2 years' experience in Quality control laboratory.
  •  Knowledge of and ability to work with equipment, supplies, components and technical areas that are utilized in the    pharmaceutical industry.
  • Knowledge of FDA guidelines on Stability requirements is a plus;
  • Must be able to analyze data and work with a high degree of accuracy; 
  • Organized and able to perform duties in a timely manner; 
  • Must be flexible and able to handle multiple activities;
  • Must have excellent computer skills and verbal and written commutation skills.
  • Must be able to work in a team environment; team player.

Additional Preferred: 

  •  Experience in GMP quality control and/or pharmaceutical manufacturing facility; 
  • Pharmaceutical stability operations experience

Physical Conditions


Long periods of sitting, standing, walking, bending, stooping, reaching, and lifting. Will work around powders and other chemicals. Protective eyewear is necessary to wear in the laboratory or manufacturing.

Requirements

Preferred Knowledge & Skills:

  • Strong knowledge of the major analytical techniques: HPLC/UPLC, GC, dissolution, etc. FT-IR, FDA/ICH regulations.
  • Solid knowledge of FDA/ICH regulations.

Required Experience & Education:

  • BS or MS in Chemistry, Pharmacy, Biochemistry, Biology or Biotechnology or related field.
  • Minimum 2 - 5 years of experience in using analytical instrument techniques including HPLC/GC/FT-IR, UV-Vis, Dissolution Apparatus, Ovens/Auto Titrators/KF Titrator/Particle size analyzers/ Ion-Chromatography.

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