The posting
"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:
- Reviews, approve and tracks executed production records.
- Reviews and approves production and QC investigations.
- Reviews lab sample results and manufacturing records related to qualification/validation activities.
- Conducts, write, and reviews quality related investigations as appropriate.
- Reviews and approves Master Production Records.
- Responsible for cGMP compliance of assigned manufacturing operations / areas.
- Completes QMS items as assigned.
- Is responsible for the conditional / 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
- Writes and reviews Product Validation / Qualification / Assessments documents.
- Writes and reviews Equipment Qualifications / Assessments documents.
- Writes and reviews Computerized Systems Validations / Assessments documents.
- Reviews, evaluates and approves minor equipment changes.
- Conducts GMP inspections.
- Conducts environmental monitoring.
- Reviews and approves CMC sections of DMFs as appropriate.
- Maintains 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.
- Adheres to all applicable SHE and cGMP 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 years of experience in QA in a pharmaceutical manufacturing environment required, or an equivalent combination of education and experience.
- Thorough knowledge of cGMP in active pharmaceutical ingredient (API) manufacturing is preferable.
Your Benefits:
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.
- The salary for this role is anticipated to be between $82,000 and $110,000
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.
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.
