layiq

/la·yiq/adjective

worthy; deserving; fitting; suitable.

A role, opportunity, or path that merits attention, time, and pursuit.

LAYIQ - In Process QA Specialist at Nivagen Pharmaceuticals LLC

Perform routine on-the-floor QA oversight within manufacturing areas, providing real-time quality support and ensuring compliance with approved procedures and GMP requirements.
Conduct line clearances, in-process checks, and verification activities during manufacturing and packaging operations.
Review and approve GMP documentation including batch production records, logbooks, sampling records, and associated manufacturing documentation.
Support deviation investigations by gathering information, participating in root cause analysis, and assisting with CAPA development and effectiveness checks.
Support the authoring, review, and approval of QA Manufacturing procedures, controlled documents, and Master Batch Records to ensure compliance with cGMP, regulatory requirements, and internal quality standards.
Participate in GMP area walkthroughs and support inspection readiness activities.
Support internal audits, regulatory inspections, and customer audits by preparing documentation and providing operational support.
Collaborate cross-functionally with Manufacturing, Engineering, Validation, and Supply Chain teams to resolve quality issues and drive continuous improvement.
Assist with product disposition activities and quality review processes under supervision.
Promote a culture of quality, compliance, and operational excellence within the organization.
Required Skills/Abilities: Strong analytical and problem-solving skills with experience in root cause analysis and CAPA implementation
High level of attention to detail, particularly in identifying quality deviations and documenting production processes
Proficiency in using quality testing equipment and familiarity with statistical process control (SPC) methods
Strong understanding of GMP, FDA regulations, and other relevant pharmaceutical industry standards
Excellent communication skills, both verbal and written, for effective collaboration and documentation
Ability to work effectively as part of a cross-functional team, including production, quality control, and regulatory affairs.
Strong organizational skills and attention to detail.
Effective written and verbal communication skills.
Ability to work independently while collaborating within cross-functional teams.
Basic knowledge of deviation management, CAPA, and change control processes preferred.
Familiarity with electronic systems such as Compliance Wire, Track Wise, SAP, LIMS, or similar eQMS platforms preferred.
Proficiency in Microsoft Office applications.
Education and Experience: Bachelor’s degree in Life Sciences, Chemistry, Engineering, or related field OR equivalent combination of education and sterile GMP manufacturing experience.
0–3 years of experience in sterile pharmaceutical, biotech, or other regulated manufacturing environments.
Working knowledge of current Good Manufacturing Practices (cGMP) and applicable FDA regulations (21 CFR).
Knowledge, Skills, and Abilities: Strong analytical and problem-solving skills with experience in root cause analysis and CAPA implementation
High level of attention to detail, particularly in identifying quality deviations and documenting production processes
Proficiency in using quality testing equipment and familiarity with statistical process control (SPC) methods
Strong understanding of GMP, FDA regulations, and other relevant pharmaceutical industry standards
Excellent communication skills, both verbal and written, for effective collaboration and documentation
Ability to work effectively as part of a cross-functional team, including production, quality control, and regulatory affairs
Job Requirements: May require working in shifts, including nights or weekends, depending on production schedules
Adherence to safety protocols, including the use of personal protective equipment (PPE) and compliance with GMP standards, is mandatory
This role requires spending significant time on the production floor, monitoring processes, and conducting tests in a cleanroom or controlled environment
Must live or willing to move to Sacramento Metropolitan Region (Approx. 40 miles’ radius)

In Process QA Specialist

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