QA Technician (2nd & 3rd Shift), Granules Pharmaceuticals, Chantilly, VA
Granules Pharmaceuticals -
Chantilly, VA,
US
QA Technician (2nd & 3rd Shift)
Date Posted: 2024-06-06
Job description
Job Type
Full-time
Description
Job Summary
The QA technician 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.
Principle Accountabilities
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.
Collaborate with team members and site customers to ensure timely deliverables for documentation.
Track controlled documents through the issuance of Document Control numbers, logbooks, change requests, and document status reports.
Management of quality documentation which includes but is not limited to number issuance, logbooks and spreadsheets.
Review of batch records and equipment logbooks.
Issue batch records, SOP's. and protocols as needed.
Assist in scanning of documents as needed.
Collect purified water and environmental samples and trend results.
Perform weekly floor audits for manufacturing.
Perform swab sampling or cleaning validation and or verification.
Ability to be flexible with working hours and weekend coverage when needed.
Any other activity as assigned by the Supervisor
Reports to
Quality Compliance manager
Physical Requirements/Working Environment
Benefits:
Company has an extensive list of initiatives implemented for employees health and overall safety in response to the COVID pandemic to ensure safe optimal working conditions for our personnel.
Requirements
Required Qualifications:
Knowledge & Skills
Experience & Education
Full-time
Description
Job Summary
The QA technician 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.
Principle Accountabilities
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.
Collaborate with team members and site customers to ensure timely deliverables for documentation.
Track controlled documents through the issuance of Document Control numbers, logbooks, change requests, and document status reports.
Management of quality documentation which includes but is not limited to number issuance, logbooks and spreadsheets.
Review of batch records and equipment logbooks.
Issue batch records, SOP's. and protocols as needed.
Assist in scanning of documents as needed.
Collect purified water and environmental samples and trend results.
Perform weekly floor audits for manufacturing.
Perform swab sampling or cleaning validation and or verification.
Ability to be flexible with working hours and weekend coverage when needed.
Any other activity as assigned by the Supervisor
Reports to
Quality Compliance manager
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.
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Disability insurance
- Employee assistance program
- Health insurance
- Health savings account
- Life insurance
- Paid time off
- Referral program
- Vision insurance
Company has an extensive list of initiatives implemented for employees health and overall safety in response to the COVID pandemic to ensure safe optimal working conditions for our personnel.
Requirements
Required Qualifications:
- Manufacturing: 2 years (Preferred)
- Document management: 2 years (Preferred)
- Quality assurance: 2 years (Preferred)
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) to three (3) years of experience in a quality assurance role in a cGMP-regulated environment.
- A college Degree preferably in sciences (i.e., Biology, Chemistry etc.)