QC Manager

Who We Are:

Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit neurocrine.com , and follow the company on LinkedIn , X , Facebook and YouTube . ( *in collaboration with AbbVie )

About the Role:

Responsible for oversight of GMP analytical testing performed by contract sites and internal GMP analytical laboratory operations. _

Your Contributions (include, but are not limited to):

Review and approve API and drug product analytical records for clinical and commercial products

Review and approve stability data supporting retest period assignment for clinical and commercial products

Review and approve internal and external test method validation protocols and reports

Review and approve equipment/instrument qualification, calibration and maintenance records to support the internal GMP lab

Participate in project teams, serving as the QC representative and escalate issues to senior Quality management when appropriate

Interact with cross-functional team members, external manufacturing sites and contract testing labs to resolve analytical testing issues

Lead or participate in deviation and laboratory investigation teams

Facilitate the change control process for analytical changes related to clinical and commercial products

Prepare reports for management review of key statistics such as vendor performance based on findings from analytical record reviews

Author and review controlled documents, including Standard Operating Procedures, analytical methods, protocols and reports related to lab activities

Author and review analytical modules in regulatory submissions

Conduct and support audits of external vendors

Assist during onsite inspections and inspection readiness activities

May lead junior staff and/or cross-functional teams

Perform additional duties as assigned by management

Requirements:

BS/BA degree in life sciences or related field AND 6+ years of experience within Pharmaceutical/Biotechnology industry OR

Master’s degree in life sciences or related field AND 4+ years of similar experience noted above

Works well in a team environment with the ability to drive results

Ability to independently meet multiple deadlines, with a high degree of accuracy and efficiency

Capable of handling multiple responsibilities and prioritizing appropriately

Strong scientific data management and organization skills with attention to detail

Ability to identify and escalate problems and follow-through with corrective actions

Ability to work closely with both internal and external personnel to increase the level of compliance and cooperation while creating opportunities to improve operations and effective implementation to reduce errors

Strong level of analysis skills to evaluate and interpret data to arrive at logical and quality-minded conclusions

Apply problem-solving tools for root cause analysis

Excellent computer skills

Strong communication skills

Leadership capabilities and experience applying CGMP requirements in a Quality Control setting

Working knowledge of quality systems and regulatory compliance requirements within a clinical and commercial drug manufacturing operation

Experience in analytical development and/or testing in a Quality Control setting

Experience with using electronic documents management systems, laboratory data management systems, document control and records management

Knowledge of US FDA and European regulations and ICH Guidelines

#LI-RS1

Neurocrine Biosciences is an EEO/Disability/Vets employer.

We are committed to building a workplace of belonging, respect, and empowerment , and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don’t line up to exactly what we have outlined in the job description.

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The annual base salary we reasonably expect to pay is $119,700.00-$164,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.