Job summary
Job post source
This job is directly from Siegfried
Job overview
The Sr. Quality Assurance Specialist at Siegfried ensures compliance with regulatory and cGMP standards in pharmaceutical manufacturing, impacting product quality and safety.
Responsibilities and impact
The role involves reviewing and approving production records and investigations, conducting audits and inspections, managing quality systems, releasing materials, and ensuring compliance with regulatory and company standards.
Compensation and benefits
The position offers a base salary of $90-97k for Sr. QA Specialist with a 5% bonus, health, dental, vision insurance, life and disability coverage, and a 401k with competitive match.
Experience and skills
Requires a BA/BS in microbiology, biology, chemistry, or engineering with 3-5 years QA experience in pharmaceutical manufacturing; knowledge of cGMP and strong communication, computer, and project management skills are essential.
Career development
Siegfried promotes personal and professional development in a dynamic, international environment with flexible and diverse career advancement opportunities.
Work environment and culture
The company culture values diversity, flexibility, and a discrimination-free environment, fostering innovation and superior performance in a motivated, professional team.
Company information
Siegfried is a leading global CDMO specializing in APIs and finished dosage forms, integrating chemical and pharmaceutical capabilities with a presence in Europe, Asia, and North America.
Job location and travel
The job is located at Siegfried's Pennsville site, a drug substance manufacturing facility serving the US market with cGMP and SHE compliant operations.
Unique job features
The role involves working at a site with advanced manufacturing capabilities including pilot and commercial scale reactors, spray drying, and micronization, supporting innovative drug substance production.
Company overview
Siegfried is a global life sciences company specializing in the development and production of active pharmaceutical ingredients (APIs) and finished dosage forms (FDFs). They generate revenue by providing comprehensive contract manufacturing and development services to pharmaceutical companies. Founded in 1873 in Zofingen, Switzerland, Siegfried has a rich history of innovation and growth, including strategic acquisitions and expansions to enhance their service offerings and global footprint. Their commitment to quality, sustainability, and regulatory compliance makes them a trusted partner in the pharmaceutical industry.
How to land this job
Tailor your resume to highlight your experience ensuring cGMP compliance, regulatory adherence, and quality assurance in pharmaceutical manufacturing, emphasizing your familiarity with FDA regulations, ICH Q7, and 21 CFR standards.
Emphasize your skills in reviewing and approving production records, investigations, validation documents, and your ability to conduct audits and inspections both internally and with regulatory authorities.
Apply to the Sr. Quality Assurance Specialist position through Siegfried's corporate career site and LinkedIn, as well as other reputable job boards that list pharmaceutical quality roles to maximize your exposure.
Connect with current Siegfried QA team members or those in the pharmaceutical manufacturing division on LinkedIn; initiate conversations by referencing Siegfried's global presence or asking about their experience with cGMP compliance and audit preparation.
Optimize your resume for ATS by incorporating keywords such as 'cGMP compliance,' 'quality assurance,' 'FDA regulations,' 'audit management,' 'validation,' and 'pharmaceutical manufacturing,' ensuring your resume matches the job description's language closely.
Utilize Jennie Johnson's Power Apply feature to automate tailoring your resume, identify multiple application portals, and find relevant LinkedIn contacts, saving you time and increasing your chances of landing an interview.
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