BioPhase Solutions
specializes in recruiting top talented professionals for Southern California's Life Sciences community. We are currently looking for an
ONSITE
temporary-to-hire
Document Management Associate
for a leading San Diego area biotech company.
*Must be local and willing to work fully onsite in San Diego, CA.
Responsibilities
Manage and maintain controlled documents and records in accordance with GMP and quality standards
Support document storage, revision control, access permissions, and archival processes
Assist with issuing batch records and controlling label stock
Support internal and external audits by providing requested documentation
Collaborate with cross-functional teams across Quality, Manufacturing, and Operations
Assist with SOP drafting, revisions, and training support as needed
Ensure document integrity, compliance, and confidentiality at all times
Qualifications
Bachelor’s degree in Biology or a related field (or equivalent experience)
1–2+ years of experience in a GMP Quality or Manufacturing environment
Familiarity with GMPs and regulated documentation practices
Experience drafting, revising, or managing controlled documents preferred
Strong attention to detail and organizational skills
Comfortable working both independently and in a team-based environment
What we offer As we work to develop innovations that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.
Full support and career-development resources to help you reach your potential
A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
#J-18808-Ljbffr
specializes in recruiting top talented professionals for Southern California's Life Sciences community. We are currently looking for an
ONSITE
temporary-to-hire
Document Management Associate
for a leading San Diego area biotech company.
*Must be local and willing to work fully onsite in San Diego, CA.
Responsibilities
Manage and maintain controlled documents and records in accordance with GMP and quality standards
Support document storage, revision control, access permissions, and archival processes
Assist with issuing batch records and controlling label stock
Support internal and external audits by providing requested documentation
Collaborate with cross-functional teams across Quality, Manufacturing, and Operations
Assist with SOP drafting, revisions, and training support as needed
Ensure document integrity, compliance, and confidentiality at all times
Qualifications
Bachelor’s degree in Biology or a related field (or equivalent experience)
1–2+ years of experience in a GMP Quality or Manufacturing environment
Familiarity with GMPs and regulated documentation practices
Experience drafting, revising, or managing controlled documents preferred
Strong attention to detail and organizational skills
Comfortable working both independently and in a team-based environment
What we offer As we work to develop innovations that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.
Full support and career-development resources to help you reach your potential
A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
#J-18808-Ljbffr