Batch Record Author Job at Page Mechanical Group, Inc. in Mainland
Page Mechanical Group, Inc., Mainland, PA, United States
Job Title: QS Associate I & II – Batch Record Auditor
Location: Mainland, PA 19451
Hours: Monday-Friday, 8:00AM-5:00PM
Join Our Team
At Accupac, we are Makers. From formulation to manufacturing, we serve the most trusted brands in the beauty and personal care industries with a wide range of cosmetics, over-the-counter and medical devices across skincare, haircare, oral care, and healthcare products.
But beyond that, we make a difference. We make a difference in the lives of our people, we make a difference in the community around us, and we make a difference in the health of our planet for a better, brighter, more beautiful future for all.
We value detail-oriented individuals who are passionate about documentation accuracy, regulatory compliance, and quality systems. As a QS Associate – Batch Record Author, you’ll play a key role in maintaining and managing the life cycle of controlled quality documents to ensure compliance with cGMP standards, company procedures, and customer requirements. From preparing and issuing templates to translating customer specifications and routing documents for approval, you’ll help ensure our quality documentation reflects current practices and supports regulatory readiness. This role is ideal for candidates who excel in communication, organization, and document control within a fast-paced manufacturing environment.
What We Offer
Competitive Pay
Salary Range: $44,000.00 - $50,000.00
Bonus: Exempt employees are eligible for a bonus in accordance with Accupac’s Bonus Plan.
The posted job may span more than one career level. The final offer, including level and pay, will be determined based on a variety of factors such as the candidate’s relevant job and industry experience, education, knowledge, skills, geographic location, and abilities. Internal equity and alignment with market data will also be considered. We are committed to providing fair and competitive compensation based on each candidate’s qualifications and fit for the role.
Employees are eligible for the following benefits:
Medical, Dental, and Vision insurance
Health Savings Account
Life Insurance with Optional Supplemental Plan
Pet InsuranceShort-Term Paid Disability
401(k) Retirement Plan with Vested Company Match Contribution
Paid Time Off (PTO)
10 Paid Holidays
Health Advocacy Programs
Career Growth
What You’ll Do
Manage the full life cycle of quality documents, including issuing templates, revising documentation, and routing for approval
Ensure all controlled documentation is compliant with cGMP, SOPs, and customer specifications
Translate customer requirements into internal documentation to support operational execution
Maintain and update paper and electronic files in accordance with Good Documentation Practices
File, archive, and scan quality documents to ensure proper traceability and accessibility
Coordinate with cross-functional teams to ensure timely document review and completion
Track progress on document revisions and elevate issues to management as needed
Support audits by preparing, organizing, and retrieving required documentation
Communicate progress, updates, and challenges clearly across various levels of the organization
Perform additional duties as assigned to support QA operations
What We’re Looking For
Bachelor’s degree required
QS Associate I: 0–2 years of Quality Assurance or Quality Control experience in a cGMP-regulated environment
QS Associate II: 2+ years of Quality Assurance or Quality Control experience in a cGMP-regulated environment
Experience with LIMS systems preferred
Working knowledge of Microsoft Office applications (Word, Excel, etc.)
Strong attention to detail, organization, and documentation accuracy
Excellent written and verbal communication skills
Ability to manage multiple priorities and meet tight deadlines
Understanding of Good Documentation Practices
Ability to lift up to 40 lbs., stand for extended periods, bend/kneel to verify components, and perform visual inspections requiring color recognition and peripheral vision
Ready to Apply
Join us at Accupac and become part of a company that values your skills and dedication. Click below to apply today!
#J-18808-Ljbffr
Location: Mainland, PA 19451
Hours: Monday-Friday, 8:00AM-5:00PM
Join Our Team
At Accupac, we are Makers. From formulation to manufacturing, we serve the most trusted brands in the beauty and personal care industries with a wide range of cosmetics, over-the-counter and medical devices across skincare, haircare, oral care, and healthcare products.
But beyond that, we make a difference. We make a difference in the lives of our people, we make a difference in the community around us, and we make a difference in the health of our planet for a better, brighter, more beautiful future for all.
We value detail-oriented individuals who are passionate about documentation accuracy, regulatory compliance, and quality systems. As a QS Associate – Batch Record Author, you’ll play a key role in maintaining and managing the life cycle of controlled quality documents to ensure compliance with cGMP standards, company procedures, and customer requirements. From preparing and issuing templates to translating customer specifications and routing documents for approval, you’ll help ensure our quality documentation reflects current practices and supports regulatory readiness. This role is ideal for candidates who excel in communication, organization, and document control within a fast-paced manufacturing environment.
What We Offer
Competitive Pay
Salary Range: $44,000.00 - $50,000.00
Bonus: Exempt employees are eligible for a bonus in accordance with Accupac’s Bonus Plan.
The posted job may span more than one career level. The final offer, including level and pay, will be determined based on a variety of factors such as the candidate’s relevant job and industry experience, education, knowledge, skills, geographic location, and abilities. Internal equity and alignment with market data will also be considered. We are committed to providing fair and competitive compensation based on each candidate’s qualifications and fit for the role.
Employees are eligible for the following benefits:
Medical, Dental, and Vision insurance
Health Savings Account
Life Insurance with Optional Supplemental Plan
Pet InsuranceShort-Term Paid Disability
401(k) Retirement Plan with Vested Company Match Contribution
Paid Time Off (PTO)
10 Paid Holidays
Health Advocacy Programs
Career Growth
What You’ll Do
Manage the full life cycle of quality documents, including issuing templates, revising documentation, and routing for approval
Ensure all controlled documentation is compliant with cGMP, SOPs, and customer specifications
Translate customer requirements into internal documentation to support operational execution
Maintain and update paper and electronic files in accordance with Good Documentation Practices
File, archive, and scan quality documents to ensure proper traceability and accessibility
Coordinate with cross-functional teams to ensure timely document review and completion
Track progress on document revisions and elevate issues to management as needed
Support audits by preparing, organizing, and retrieving required documentation
Communicate progress, updates, and challenges clearly across various levels of the organization
Perform additional duties as assigned to support QA operations
What We’re Looking For
Bachelor’s degree required
QS Associate I: 0–2 years of Quality Assurance or Quality Control experience in a cGMP-regulated environment
QS Associate II: 2+ years of Quality Assurance or Quality Control experience in a cGMP-regulated environment
Experience with LIMS systems preferred
Working knowledge of Microsoft Office applications (Word, Excel, etc.)
Strong attention to detail, organization, and documentation accuracy
Excellent written and verbal communication skills
Ability to manage multiple priorities and meet tight deadlines
Understanding of Good Documentation Practices
Ability to lift up to 40 lbs., stand for extended periods, bend/kneel to verify components, and perform visual inspections requiring color recognition and peripheral vision
Ready to Apply
Join us at Accupac and become part of a company that values your skills and dedication. Click below to apply today!
#J-18808-Ljbffr