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Flexible Generic Pharma Jobs (NOW HIRING)

Granules Pharmaceuticals

Trainee Engineer

Chantilly, VA · On-site

$23 - $25/hr

... fastest growing generic pharma company in the US! With our sites in Chantilly and Manassas ... Hours are flexible depending on business needs based on production/R&D process workflow and may ...

Granules

Trainee Engineer

Chantilly, VA · On-site

... fastest growing generic pharma company in the US! With our sites in Chantilly and Manassas ... Hours are flexible depending on business needs based on production/R&D process workflow and may ...

New

Loxo CS Demo

Associate Dir of Sales

Denver, CO

Bigtime PHARMA LOCATION: BOULDER, CO (HQ) - CANDIDATE LOCATION FLEXIBLE COMPANY OVERVIEW : Bigtime ... Route Scouting & Process Development for Proprietary and Generic APIs * High Potency API Contract ...

Abbott

$62K - $80K/yr

Internship or co-op in regulated manufacturing (medical devices/pharma) * Exposure to Lean ... Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter ...

Sun Pharmaceutical Industries

IL

$64K - $79K/yr

Driven by a bold pursuit of science and fueled by an unwavering commitment to patients, Sun Pharma ... Generic Rx sales. Responsibilities: * Monitor daily order flow and sales activity, ensuring the ...

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Flexible Generic Pharma information

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$31K

$48.2K

$97K

How much do flexible generic pharma jobs pay per year?

As of Aug 4, 2026, the average yearly pay for flexible generic pharma in the United States is $48,183.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,500.00 and $57,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a pharmaceutical sales representative?

To excel as a Pharmaceutical Sales Representative, you need a bachelor's degree (often in life sciences or business), strong product knowledge, and excellent sales acumen. Familiarity with CRM software and knowledge of pharmaceutical regulations are typical technical requirements. Outstanding interpersonal skills, persuasive communication, and resilience help you build strong relationships with healthcare professionals. These skills ensure you can effectively promote products, meet sales targets, and maintain compliance in a highly regulated industry.

What is a flexible generic pharma professional?

A Flexible Generic Pharma professional typically works in the pharmaceutical industry, focusing on the development, production, or distribution of generic drugs while adapting to various roles and responsibilities. This flexibility can include working in regulatory affairs, quality assurance, research and development, or supply chain management. The role requires a strong understanding of pharmaceutical regulations, manufacturing processes, and market demands. Flexible Generic Pharma professionals are valued for their ability to quickly adapt to new challenges and projects across the generic drug sector.

How does working in a flexible generic pharma role differ from positions in branded pharmaceutical companies?

In a Flexible Generic Pharma role, professionals typically work in a fast-paced environment focused on cost-effective production, regulatory compliance, and rapid product development to compete with other generic manufacturers. Daily tasks often involve cross-functional collaboration with regulatory, quality assurance, and R&D teams to ensure products meet regulatory standards and reach market quickly. The team structure tends to be lean, requiring adaptability and strong communication skills. Unlike branded pharma, there's a greater emphasis on efficiency, process optimization, and responding to market changes. This environment offers valuable experience in multiple facets of pharmaceutical operations and can provide opportunities for rapid career progression.

What is the difference between Flexible Generic Pharma vs Contract Manufacturing Associate?

AspectFlexible Generic PharmaContract Manufacturing Associate
CredentialsRelevant degrees in pharmacy, chemistry, or pharmaceutical sciencesSimilar educational background, often with industry certifications
Work EnvironmentPharmaceutical manufacturing facilities, quality control labsManufacturing plants, production lines, quality assurance areas
Industry UsageDeveloping and producing flexible generic medicinesSupporting manufacturing processes for various pharmaceutical products

Flexible Generic Pharma and Contract Manufacturing Associate roles both require pharmaceutical knowledge and work in manufacturing environments. While Flexible Generic Pharma focuses on developing and producing flexible generic medicines, Contract Manufacturing Associates support the production processes across different pharmaceutical products. Both roles are essential in the pharmaceutical industry, often overlapping in skills and work settings.

More about Flexible Generic Pharma jobs
What cities are hiring for Flexible Generic Pharma jobs? Cities with the most Flexible Generic Pharma job openings:
What are the most commonly searched types of Generic Pharma jobs? The most popular types of Generic Pharma jobs are:
What states have the most Flexible Generic Pharma jobs? States with the most job openings for Flexible Generic Pharma jobs include:
What job categories do people searching Flexible Generic Pharma jobs look for? The top searched job categories for Flexible Generic Pharma jobs are:
Flexible Generic Pharma jobs near you
Infographic showing various Flexible Generic Pharma job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 66% Full Time, 30% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $48,183 per year, or $23.2 per hour.

QC Lab Tech (Stability Coordinator) (Pharmaceutical Manufacturing)

Granules Pharmaceuticals

Chantilly, VA

$19 - $22/hr

Other

Re-posted 3 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.


We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.



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