Sr. Quality Assurance Specialist

Siegfried AG; Pennsville Township (NJ); On-site; USD 82,000 - 110,000; Full time

Benefits offered by this job

Accommodations available

Job summary

Siegfried USA, LLC is seeking a QA professional to ensure regulatory compliance, cGMP adherence, and systematized quality oversight across manufacturing operations.

The role emphasizes review and approval of production records, investigations, and validation activities, with responsibilities spanning interactions during internal and regulatory audits and annual product reviews. Candidates should have a BA/BS in a scientific field and 3–5 years in pharmaceutical QA.

Qualifications

• Bachelor’s degree in a relevant science or engineering field required with 3–5 years of QA experience in pharmaceutical manufacturing.
• Excellent communication skills are essential for cross‑functional collaboration.
• Ability to manage priorities, deadlines and multiple projects autonomously.

Responsibilities

• Review, approve and track executed production records and change controls.
• Review and approve production and QC investigations and related CAPAs.
• Review lab results and manufacturing records related to qualification/validation activities.
• Write, review and approve product quality and process validation/qualification documents.
• Maintain QA databases and ensure cGMP compliance for assigned operations.

Skills

Communication

Detail orientation

Team player

Self-management

Project management

Deadline adherence

Education

BA/BS in microbiology/biology/chemistry/engineering

Job description

Company Overview:

"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions-offering long-term opportunities to grow and make an impact.

Your Role:

The incumbent assures compliance to all regulatory requirements, current Good Manufacturing Practices, and company Policies, Standard Operating Procedures and Work Instructions.

Your Profile:

ESSENTIAL DUTIES, RESPONSIBILITIES AND ACCOUNTABILITIES :

• Review s , approve and track s executed production records.


• Review s and approve s production and QC investigations.


• Review s lab sample results and manufacturing records relat ed to qualification/validation activities.


• Conduct s , write, and review s quality related investigations as appropriate .


• Review s and approve s Master Production Records.


• Responsible for cGMP compliance of assigned manufacturing operations / areas.


• Complete s QMS items as assigned.


• Is responsible for the c onditional / final release of materials.


• Hosts customer and internal audits, as needed


• Conduct internal and external audits, as needed


• Participates in inspections by regulatory authorities


• Writes and reviews Annual Product Reviews/Product Quality Reviews


• Write s and review s Product Validation / Qualification / Assessments documents .


• Write s and review s Equipment Qualifications / Assessments documents.


• Write s and review s Computerized Systems Validations / Assessments documents.


• Review s , evaluates and approve s minor equipment changes .


• Conduct s GMP inspections .


• Conducts e nvironmental monitoring.


• Review s and approve s CMC sections of DMFs as appropriate .


• Maintain s QA databases for products / equipment as appropriate .


• Adheres to personal moral, ethical, legal, and behavioral conduct that is in compliance with the Siegfried Code of Conduct.


• Adhere s to all applicable SHE and c GMP regulations e.g. ICH Q7, FDA, 21 CFR 210 and 211, etc .

EDUCATION AND EXPERIENCE:

A BA/BS degree in microbiology, biology, chemistry, or engineering and 3-5 y ears of experience in QA in a pharmaceutical manu facturing environment required , or an equivalent combination of education and experience.

OTHER REQUIREMENTS:

• Must have excellent communication skills.


• Must be conscientious and detail oriented .


• Must have excellent computer skills (MS Office 365 ).


• Must be a team player.


• Must be able to self- manage daily work and set priorities.


• Must be able to manage projects and prioritize appropriately.


• Must be able to adhere to deadlines.

Salary:

The salary for this role is anticipated to be between $82,000 and $110,000

Accommodations:

Siegfried USA , LLC will explore and provide reasonable accommodations to assist any qualified individual with a disability in performing the essential functions of his/her job. Please speak with HR should you require an accommodation or have any questions.

About the company:

Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 13 sites across three continents. With a team of more than 3,800 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry.