QA Associate - Pharmaceutical Manufacturing

Granules Pharmaceuticals, Inc.; Manassas (VA); On-site; USD 55,000 - 65,000; Full time

Job summary

Granules Consumer Health, LLC in Manassas, VA seeks a QA Associate for Documentation to ensure cGMP compliance and support regulatory alignment. You will perform inspections, batch record reviews, and uphold quality systems in accordance with SOPs, state and federal laws.

Applicants should have at least two years in a quality assurance role within a cGMP environment and a Science-related degree. The role includes collaboration with cross-functional teams and involvement in documentation control

Qualifications

• cGMP compliance knowledge in pharma manufacturing.
• Proficiency in writing and maintaining cGMP documentation.
• Ability to analyze data to resolve issues.
• Strong verbal and written communication skills.

Responsibilities

• Manage document control systems and archival in compliance with procedures and regulatory requirements.
• Route, review, approve, distribute, and archive controlled documents.
• Track documents with control numbers, logs, change requests and reports.
• Maintain batch records, audit files, vendor files, labels and change histories.
• Control labeling components and document control logbooks/spreadsheets.
• Facilitate release of finished product batches for packaging.
• Provide new hire training on GMP, safety, and pharmacovigilance; maintain training docs.
• Ensure SOPs are current and relevant; collaborate to meet timelines.

Skills

cGMP compliance

Documentation writing

Data analysis

Verbal & written comms

Cross-functional collab

Multi-tasking

Education

Bachelor's degree in Sciences

Job description

Description

Granules Consumer Health, LLC is a subsidiary of Granules India LTD, a vertically integrated pharmaceutical company with headquarters in Hyderabad, India. Granules Consumer Health, LLC is located in Manassas, Virginia. We have over 106 employees and annual revenue of $76.64 million. We serve as Granules’ packaging facility and front-end division for private label over the counter (OTC) products in the US. We offer OTC generics that meet the highest level of quality at an affordable cost. As such, we are well-established on bulk supply through efficiencies garnered through manufacturing, integration and a high level of regulatory compliance. We are dedicated to excellence in manufacturing, quality, and customer service.

Job Type

Full-time

Description

Granules Consumer Health, LLC is a subsidiary of Granules India LTD, a vertically integrated pharmaceutical company with headquarters in Hyderabad, India. Granules Consumer Health, LLC is located in Manassas, Virginia. We have over 106 employees and annual revenue of $76.64 million. We serve as Granules’ packaging facility and front-end division for private label over the counter (OTC) products in the US. We offer OTC generics that meet the highest level of quality at an affordable cost. As such, we are well-established on bulk supply through efficiencies garnered through manufacturing, integration and a high level of regulatory compliance. We are dedicated to excellence in manufacturing, quality, and customer service.

The QA associate for documentation ensures compliance with cGMP and internal policies, procedures, and specifications. This position is responsible for performing inspections, batch record review, and quality system functions in accordance with cGMP and related company SOP’s, state, federal and local laws as applicable. This person should be knowledgeable of cGMP requirements, FDA regulations and ICH guidelines.

Job Duties & Responsibilities

• Manage and maintain company document control and archival systems (hardcopy and electronic) in compliance with internal procedures and policies as well as regulatory requirements.
• Manage the routing, review, approval, distribution and archival of new and revised controlled documents.
• Track controlled documents through the issuance of Document Control numbers, logbooks, change requests, and document status reports.
• Archive and maintain hardcopy and electronic copies of batch records files, audit files, vendor files, product, label files and change history files.
• Control and issuance of labeling components.
• Manage all document control logbooks and spreadsheets.
• Perform the release of finished product batches packaged.
• Provide new hire training on GMP’s, Safety, and Pharmacovigilance and maintain the training program documentation.
• Ensure standard operating procedures are periodically reviewed for relevance and accuracy in compliance with company policies and procedures.
• Collaborate with team members to ensure timely deliverables for documentation.
• Ensuring all documents are up to date with respect to version control and issuance
• Perform and support maintenance and closure activities of documents such as reports, protocols exceptions/deviations, CAPAs, change controls and complaints.
• cGMP Compliance in Document Control.
• Any other activity as assigned by the Supervisor

Requirements

Knowledge & Skills

• cGMP compliance within the pharmaceutical manufacturing industry.
• Writing and maintaining cGMP documentation.
• Analyze data/information and resolve complex issues.
• Verbal and written communication skills.
• Work and communicate with cross-functional teams.
• Multiple priorities and re-prioritize tasks.

Experience & Education

• At least two (2) years’ experience in a quality assurance role in a cGMP-regulated environment.
• A college Degree preferably in Sciences (i.e. Pharmacy, Biology, Chemistry etc.)

Physical Requirements/Working Environment

• While performing the duties of this job, the employee is regularly required to, stand, sit, talk, hear, and use hands and fingers to operate a computer and telephone keyboard.
• Specific vision abilities required by this job include close vision requirements due to computer work.
• Ability to sit at a computer terminal for an extended period of time.
• Light to moderate lifting up to 10-15 lbs. is required.
• Ability to work in a confined area.

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

Salary Description

$55,000 - $65,000 per year