Quality Manger - Dietary Supplements
Symphony Natural Health Symphony Natural Health West Valley City, UT West Valley City, UT Part-time Part-time $75,000 - $85,000 a year $75,000 - $85,000 a year 4 days ago 4 days ago 4 days ago About Symphony Natural Health:
Please read more about us on our website:
www.
symphonynaturalhealth.
com The Quality Manager is responsible for managing all aspects of quality control, quality assurance, and document control to ensure compliance with local, state, and federal regulations and industry standards (21 CFR 111, UDAF, HACCP, FSMA etc.
) for dietary supplement manufacturing, warehousing, and distribution.
The Quality Manager oversees developing, implementing and maintaining quality programs, policies and procedures.
Essential Job Functions Compliance:
o Manage quality systems to ensure compliance with all applicable regulations and standards from governments and third-party certification agencies.
(cGMP/FDA, HACCP, Kosher, Organic, FSMA, NSF, TGA, etc.
) o Manager review and approval of MBRs and MMRs at each step of production process Documentation:
Oversee document control functions.
o Responsible for ensuring Product Specification and COAs, and other documents are current and updated and cGMP SOPs are reviewed, and revised following revision control procedures.
o Support in writing, reviewing, and completing assorted questionnaires submitted by international customers.
o Support accuracy of inventory records through regular review and audit Testing:
Manage and document product testing with third party laboratories in accordance with established specifications for incoming, in-process and finished goods.
Investigating & Reporting:
Management around non-conformances, CAPA reports, deviations, OOS testing, complaints, etc.
Facility Compliance:
Oversee sanitation and pest control programs.
Audits:
Perform regular internal audits to ensure compliance with SOPs and applicable requirements and regulations.
Participate in external audits as applicable.
Training and Education:
In conjunction with department managers, coordinate cGMP, SOP and replated employee training.
Other/General:
Perform other duties inherent of the position and any additional tasks required.
Qualifications
Experience:
Minimum 5
years' experience working in Quality in an FDA regulated industry (Nutraceuticals, Food or Pharma) Regulatory/Third Party Audit Experience Required 21 CFR 111 Expertise Proficiency in Microsoft Office and Adobe Education and Training:
BS or higher Sciences or Technical Degree Must be GMP trained or Certified Quality Certifications a plus (PCQI, CQA etc.
) Bilingual (Spanish) a plus Job Type:
Part-time Pay:
$75,000.
00 - $85,000.
00 per year
Benefits:
401(k) 401(k) matching Employee discount Flexible schedule Paid time off Experience level:
5 years Schedule:
Monday to Friday Work setting:
In-person Manufacturing facility Office Warehouse
Experience:
Dietary Supplement cGMP:
5 years (Required) Language:
Spanish (Preferred) Work Location:
In person.
Estimated Salary: $20 to $28 per hour based on qualifications.
Please read more about us on our website:
www.
symphonynaturalhealth.
com The Quality Manager is responsible for managing all aspects of quality control, quality assurance, and document control to ensure compliance with local, state, and federal regulations and industry standards (21 CFR 111, UDAF, HACCP, FSMA etc.
) for dietary supplement manufacturing, warehousing, and distribution.
The Quality Manager oversees developing, implementing and maintaining quality programs, policies and procedures.
Essential Job Functions Compliance:
o Manage quality systems to ensure compliance with all applicable regulations and standards from governments and third-party certification agencies.
(cGMP/FDA, HACCP, Kosher, Organic, FSMA, NSF, TGA, etc.
) o Manager review and approval of MBRs and MMRs at each step of production process Documentation:
Oversee document control functions.
o Responsible for ensuring Product Specification and COAs, and other documents are current and updated and cGMP SOPs are reviewed, and revised following revision control procedures.
o Support in writing, reviewing, and completing assorted questionnaires submitted by international customers.
o Support accuracy of inventory records through regular review and audit Testing:
Manage and document product testing with third party laboratories in accordance with established specifications for incoming, in-process and finished goods.
Investigating & Reporting:
Management around non-conformances, CAPA reports, deviations, OOS testing, complaints, etc.
Facility Compliance:
Oversee sanitation and pest control programs.
Audits:
Perform regular internal audits to ensure compliance with SOPs and applicable requirements and regulations.
Participate in external audits as applicable.
Training and Education:
In conjunction with department managers, coordinate cGMP, SOP and replated employee training.
Other/General:
Perform other duties inherent of the position and any additional tasks required.
Qualifications
Experience:
Minimum 5
years' experience working in Quality in an FDA regulated industry (Nutraceuticals, Food or Pharma) Regulatory/Third Party Audit Experience Required 21 CFR 111 Expertise Proficiency in Microsoft Office and Adobe Education and Training:
BS or higher Sciences or Technical Degree Must be GMP trained or Certified Quality Certifications a plus (PCQI, CQA etc.
) Bilingual (Spanish) a plus Job Type:
Part-time Pay:
$75,000.
00 - $85,000.
00 per year
Benefits:
401(k) 401(k) matching Employee discount Flexible schedule Paid time off Experience level:
5 years Schedule:
Monday to Friday Work setting:
In-person Manufacturing facility Office Warehouse
Experience:
Dietary Supplement cGMP:
5 years (Required) Language:
Spanish (Preferred) Work Location:
In person.
Estimated Salary: $20 to $28 per hour based on qualifications.
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