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Full Time Anda Jobs (NOW HIRING)

Kettering Health

Radiopharmacist - PET

Kettering, OH

Job Details PET | Kettering | Full-time | First Shift Responsibilities & RequirementsThe Nuclear ... ANDA, INDA's. Minimum Education * Master's degree in nuclear pharmacy Required Licenses * [United ...

Kettering Health

Radiopharmacist - PET

Kettering, OH

Incentives PET | Kettering | Full-time | First Shift Overview Kettering Health is a not-for-profit ... include ANDA, INDA's. Minimum Education * Master's degree in nuclear pharmacy Required Licenses ...

Kettering Health

Radiopharmacist - PET

Kettering, OH · On-site

PET | Kettering | Full-time | First Shift The Nuclear Pharmacist for the Nuclear Medicine/ PET ... ANDA, INDA's.   Minimum Education * Master's degree in nuclear pharmacy Required Licenses ...

Kettering Health

Radiopharmacist - PET

Kettering, OH · On-site

Job Details PET | Kettering | Full-time | First Shift Responsibilities & Requirements The Nuclear ... ANDA, INDA's. Minimum Education * Master's degree in nuclear pharmacy Required Licenses * [United ...

MITER Brands

Yard Jockey - Hegins Plant

Hegins, PA · On-site

$22.65/hr

Yard JockeyOpportunity at MI Windows and Doors in Hegins! FULL-TIME - 2 nd Shift;Mon-Fri 2:30pm ... Have a customer service mentality anda strong desireto meet daily production goalssothe ...

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Full Time Anda information

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How much do full time anda jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for full time anda in the United States is $17.50, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $18.99 per hour, depending on experience, location, and employer.

What is the difference between Full Time Anda vs Part Time Anda?

AspectFull Time AndaPart Time Anda
Work HoursTypically 35-40 hours/weekLess than 30 hours/week
Employment StatusFull employment benefits, stabilityLess benefits, flexible schedule
CredentialsUsually the same certificationsSame certifications often required
Work EnvironmentConsistent, office or remoteFlexible, part-time settings

Full Time Anda offers stable employment with full benefits and consistent hours, ideal for those seeking job security. Part Time Anda provides flexibility with fewer hours and benefits, suitable for students or those needing a secondary income. Both roles often require similar credentials and work in comparable environments, but differ mainly in hours and benefits.

More about Full Time Anda jobs
What cities are hiring for Full Time Anda jobs? Cities with the most Full Time Anda job openings:
What are the most commonly searched types of Anda jobs? The most popular types of Anda jobs are:
What job categories do people searching Full Time Anda jobs look for? The top searched job categories for Full Time Anda jobs are:
Full Time Anda jobs near you
Infographic showing various Full Time Anda job openings in the United States as of July 2026, with employment types broken down into 39% Locum Tenens, 13% Internship, 38% Full Time, 4% Part Time, 2% Nights, and 4% Summer. Highlights an 95% Physical, 3% Hybrid, and 2% Remote job distribution, with an average salary of $36,392 per year, or $17.5 per hour.

Formulation Scientist (Solid Orals)

Granules Pharmaceuticals

Chantilly, VA • On-site

$100K - $110K/yr

Full-time

Re-posted 20 days ago

Job description

Job Type
Full-time
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
  • Under general direction, manages, plans, and executes projects for product development.
  • Under limited direction and supervision, carries out design and development of solid oral dosage forms using quality by design (QbD concept) through ANDA filing and/or product launch.
  • Under limited direction and supervision, carries out design and development of complex oral dosage forms using QbD concepts through ANDA filing and/or product launch.
  • Develops and executes formulation strategies related to product development (i.e., project planning and timelines, experimental design, data evaluation, formulation of relevant and scientifically based conclusions
  • Coordinates studies with other technical groups (i.e., Analytical Sciences, Biopharmaceutics, Legal, Regulatory & Tech Services).
  • Maintains a high level of expertise within the field and develops new technologies and concepts to be applied in the development of oral controlled release drug products.
  • Participates as a project leader, manager and/or ad hoc member in Product Development efforts, and identifies, analyzes and suggests corrective actions to optimize R&D processes, technology and regulatory compliance issues.

Principal Accountabilities
  • Developing pharmaceutical products, leading to successful ANDA filings and approval in a timely manner.
  • Managing and scheduling multiple projects, setting objectives, prioritizing activities to meet the milestones in a fast-paced environment.
  • Designing, formulation and process development for various drug from project initiation to commercialization by following appropriate GMP regulations and safety requirements.
  • Participate in the set-up and operation of pilot scale equipment and instrumentation for the completion of small production runs in collaboration with the R&D technician.
  • Design and conduct pre-formulation and formulation studies, process development and optimization of prescription dosage form designs and ANDA oral Dosage forms using DOE
  • Perform Literature search and Evaluate patents to develop non-infringing strategies
  • Preparation of product manufacturing, batch records and protocols for different product development stages, including from R&D prototype formulations to process validations following SOPs and procedures, ensuring the detailed record and data keeping.
  • Utilize formulation techniques, processing equipment and unit operations including Wurster Coating, Tablet Coating, Compression, Blending, Encapsulation, HPLC, Spectrophotometry, Dissolution, Viscometer to develop Bio-Equivalent products
  • Review Analytical Data, draft SOP's, Process Evaluation protocols, IQ, OQ, PQ protocols and GMP Manufacturing Batch records, Packaging Batch Records.
  • Characterization of APIs, excipients and in process products; analysis of in-process samples or in-process products based on protocols and QbD concept, preparing various formulation samples to support cross-functional programs as needs.
  • Completes documentation associated with manufacturing processes (e.g. batch record, protocols, and logbooks) with detail and accuracy.
  • Establishing documentation management systems for CMC development and meeting FDA GMP, regulatory requirement, and FDA onsite inspections.
  • Comprehensive knowledge of IVIVC, QbD and Design of Experiments (DOE).
  • Ensuring all regulatory documents in compliance with SOPs, FDA Regulations, and cGMP policy where applicable.
  • Knowledge of manufacturing regulatory programs and objectives (cGMP, CFR 210 and 211).
  • Maintaining compliance with GMP, SOPs and DEA regulations.
  • Coordinate with Regulatory Affairs, Operations, QC/QA and Supply Departments to ensure that projects are planned and executed in a timely manner.

Management Responsibility
The Senior Scientist leads the assigned projects and guides the operation of the product development ranging from selection of staff, choice of methods, purchase of equipment, quality assurance, quality control, safety, hours of operation, scheduling of staff, and utilization management.
Reports to
Sr. Vice President, R&D
Requirements
Minimum Requirements
Knowledge & Skills Good communication skills, critical thinking, flexibility, time management, self-motivation.
Minimum Experience & Education
  • Ph.D. in pharmaceutical sciences with minimum of 2 years' experience OR;
  • Masters in pharmaceutical sciences with minimum of 5 year' experience in generic product development, with emphasis in solid/liquid orals or an equivalent combination of education and experience.

Disclaimer: The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.
We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.
Salary Description
$100,000 - $110,000 per year

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