What are the responsibilities and job description for the Quality Assurance Manager, Finished Goods position at Planet Pharma?
Key Responsibilities
Serve as QA representative for commercial finished goods and external manufacturing partners.
Represent Finished Goods Quality Operations at routine internal meetings and external contract manufacturers and for commercial production.
Oversee quality aspects of commercial finished goods specifications, qualification and validation, drawings, artwork, label, serialization, and packaging operations at CMOs for global commercial supply and ensure compliance to internal standards and regulatory requirements for US production.??
Review and approval of content within manufacturing partner and Alnylam Label and Pack documents, including BOMs, MPRs, Product Specifications, and Variable Data.
Ensure proper archival of manufacturing partner documentation in Alnylam’s document management system.
Manage Quality Records (deviation, capa, change control, serialization excursions, issue escalation) as it relates to commercial finished good assembly, label, and packaging activities.?
Recommend continuous improvement opportunities on an ongoing basis to proactively mitigate current and future risks to maintain an effective operation to support business needs.?
Qualifications
Minimum BS degree in life sciences, engineering, or related field.?
A minimum of 5 years of experience in a pharmaceutical or biopharmaceutical company.?
Experience with finished goods assembly, labeling, and packaging manufacturing operations at external manufacturers.
Excellent organizational, communication (written and verbal), and interpersonal skills.
Experience leading, training, and/or implementing root cause analysis and effective investigation practices.?
Pay ranges between $70-75/hr based on experience
Serve as QA representative for commercial finished goods and external manufacturing partners.
Represent Finished Goods Quality Operations at routine internal meetings and external contract manufacturers and for commercial production.
Oversee quality aspects of commercial finished goods specifications, qualification and validation, drawings, artwork, label, serialization, and packaging operations at CMOs for global commercial supply and ensure compliance to internal standards and regulatory requirements for US production.??
Review and approval of content within manufacturing partner and Alnylam Label and Pack documents, including BOMs, MPRs, Product Specifications, and Variable Data.
Ensure proper archival of manufacturing partner documentation in Alnylam’s document management system.
Manage Quality Records (deviation, capa, change control, serialization excursions, issue escalation) as it relates to commercial finished good assembly, label, and packaging activities.?
Recommend continuous improvement opportunities on an ongoing basis to proactively mitigate current and future risks to maintain an effective operation to support business needs.?
Qualifications
Minimum BS degree in life sciences, engineering, or related field.?
A minimum of 5 years of experience in a pharmaceutical or biopharmaceutical company.?
Experience with finished goods assembly, labeling, and packaging manufacturing operations at external manufacturers.
Excellent organizational, communication (written and verbal), and interpersonal skills.
Experience leading, training, and/or implementing root cause analysis and effective investigation practices.?
Pay ranges between $70-75/hr based on experience
Salary : $70 - $75