What are the responsibilities and job description for the Corporate Quality Assurance Manager position at MP Biomedicals?
MP Biomedicals is dedicated to giving scientists and researchers innovative, quality tools and superior service to aid them in their quest for ground-breaking discovery and turning the hope for life-changing solutions into a reality.
The company manufactures and sells more than 55,000 products and is one of the only companies in the industry to offer a comprehensive line of life science, fine chemical and diagnostic products.
Working at MP Biomedicals
At MP Biomedicals, we are striving to make the world a better place. Whether your work has you developing innovative new products, supporting customers to keep their projects on track, or delivering diagnostic solutions, our team comes together to help advance scientific discovery.
We foster an environment of teamwork and creativity, but also value the importance of your unique talents and contributions. Join MP Biomedicals today to advance your career and help make the world a better place.
Working at MP Biomedicals
At MP Biomedicals, we are striving to make the world a better place. Whether your work has you developing innovative new products, supporting customers to keep their projects on track, or delivering diagnostic solutions, our team comes together to help advance scientific discovery.
We foster an environment of teamwork and creativity, but also value the importance of your unique talents and contributions. Join MP Biomedicals today to advance your career and help make the world a better place.
Primary Function
The QA Manager coordinates and will participate in the quality activities for both Life Science and Diagnostic sections.
Principal Duties and Responsibilities
- Conduct the oversight for processes and procedures related to ISO9001 and ISO13485
- Review the risk assessments of our processes and procedures related to ISO9001 and ISO13485
- Coordinate, lead and review validation plan, protocols, and all related validation documents
- Perform all QA activities (trouble report tracking, customer complaint investigation, daily QA checking, supplier qualification, customer audit, ISO (re)certification and internal audit, CAPA and Supplier Review Board (SRB) meeting, change control…) in compliance with our Standard Operating Procedures (SOP’s)
- Ensure our QA records are clear and implementation activities are effective and timely
- Prepare customer questionnaires, forms and other quality related documents
- Provide QA support for marketing and new product development projects, including new product launch
- In line with business requirements, these responsibilities may expand or otherwise include additional areas of responsibility as assigned.
- Other duties as assigned or deemed necessary for role
Preferred Education and Experience
- Bachelor’s degree in Science or Engineering related field preferred
- At least 5 years’ experience working in the pharmaceutical or biotechnology industry required
- Experience working in ISO9001 and ISO13485 standards highly preferred
- Proven work history demonstrating strong communication and collaboration skills
- History of working with limited supervision, exercising a high level of autonomy in completing work tasks within scheduled times and according to work procedures.
In Addition to Very Competitive Wages, MP Biomedicals offers a comprehensive list of benefits including:
- Childcare Credit- $100 per month, per child
- Employee Referral Program- $1000 available for all positions
- Paid Vacation Time and Paid Time Off
- 10 Paid Holidays Per Year
- 401k with company matching contributions
- Very competitive healthcare benefits offering
- Opportunities to develop personally and professionally
- And so much more…
Job Type: Full-time
Benefits:
- 401(k) matching
- Dental insurance
- Employee assistance program
- Employee discount
- Health insurance
- Health savings account
- Life insurance
- Paid time off
- Professional development assistance
- Referral program
- Vision insurance
Schedule:
- 8 hour shift
- Monday to Friday
Supplemental Pay:
- Bonus pay
Ability to commute/relocate:
- Solon, OH 44139: Reliably commute or planning to relocate before starting work (Required)
Experience:
- ISO 13485: 1 year (Required)
Work Location: One location
