Associate Director, Stability Management

Exelixis; Alameda (CA); On-site; USD 172,000 - 244,000; Full time

Benefits offered by this job

401k plan

Medical/dental/vision coverage

Life insurance

Disability insurance

Stock purchase program

Discretionary annual bonus

Job summary

Exelixis is seeking an Associate Director of Stability Management to lead the stability group within the CMC organization. You will oversee stability programs for drug substance, drug product, and reference standards across commercial and clinical programs, while partnering with CMOs to ensure protocol adherence and data integrity.

The role requires strong leadership, technical writing, and statistical analysis skills, with responsibilities spanning policy development, performance metrics, and

Qualifications

• GMP experience preferred.
• Technical laboratory experience in small molecules and solid oral dosage forms preferred.
• Experience in the pharmaceutical industry preferred.

Responsibilities

• Establish stability policies and procedures.
• Oversee the stability program and metrics.
• Supervise stability group staff and performance reviews.
• Write/review stability protocols per ICH guidelines.
• Manage contract labs and review stability data.
• Generate stability reports and COAs.

Skills

GMP experience

Technical laboratory experience

Pharmaceutical industry experience

Education

BS/BA in related discipline

MS/MA in related discipline

PhD in related discipline

Job description

SUMMARY/JOB PURPOSE

The Associate Director, Stability Management is responsible for the establishment and management of the stability group within Exelixis CMC department. This role oversees the overall strategy and oversight of Exelixis' stability and reference standard programs for drug substance, drug product and reference standard for both the commercial and clinical programs. Additional responsibilities include establishing Exelixis stability policies, procedures, and performance metrics internally and externally with CMOs. Will provide oversight over the CMOs' execution of the stability studies, authoring of the stability protocols, interim stability reports, and final stability reports. This role requires strong personnel resource management, communications, technical writing, and statistical analysis skills.

ESSENTIAL DUTIES AND RESPONSIBILITIES

• Establish Exelixis stability policies and procedures
• Establish and manage performance metrics
• Oversee direct reports from the stability group

MANAGE ACTIVITIES RELATED TO DRUG SUBSTANCE AND DRUG PRODUCT STABILITY TESTING, BOTH COMMERCIAL AND CLINICAL

• Write and review stability protocols according to International Conference on Harmonization (ICH) guidelines.
• Manage and monitor contract laboratory stability testing to ensure adherence to the stability scheduled outlined in the stability protocols.
• Review stability data (including raw test data).
• Trend and track stability data and to determine drug product shelf life/retest date according to ICH guidelines.
• Investigate out of trend or out of specification results according to industry best practices.
• Manage, chair and present in regularly scheduled stability committee meetings.
• Write final stability reports for completed stability studies.
• Review and assess temperature excursions during storage and/or during transportation.
• Generate certificate of analysis and retest memos, setting and justifying specifications for both release and stability testing, and regulatory document controls.

SUPERVISORY RESPONSIBILITIES

• Supervise staff, including hiring, scheduling, and assigning work, reviewing performance, and recommends salary increases, promotions, transfers, demotions, or terminations.
• Provide direction to other individuals.

EDUCATION / EXPERIENCE / KNOWLEDGE & SKILLS

EDUCATION/EXPERIENCE

• BS/BA degree in related discipline and a minimum of eleven years of related experience; or,
• MS/MA degree in related discipline and a minimum of nine years of related experience; or,
• PhD degree in related discipline and a minimum of five years of related experience; or,
• Equivalent combination of education and experience.

EXPERIENCE / THE IDEAL FOR SUCCESSFUL ENTRY INTO JOB

• GMP experience preferred
• Technical laboratory experience in small molecules and solid oral dosage preferred.
• Experience in Pharmaceutical industry preferred.

KNOWLEDGE/SKILLS

• Has extensive experience in relevant industry/profession and area of specialization.
• Uses professional concepts and company objectives to resolve complex issues in creative and effective ways.
• Identifies and implements methods and procedures to achieve results.
• Performs a variety of complicated tasks with a wide degree of creativity and latitude.
• Has complete understanding and wide application of technical principles, theories, concepts, and techniques.
• Has good general knowledge of other related disciplines.
• Applies strong analytical and business communication skills.

WORKING CONDITIONS

Environment: primarily working indoors in an office environment
Travel required - 10% of travel required

#LI-MB1

Our compensation reflects the cost of labor across several U.S. geographic markets, and we pay differently based on those defined markets. The base pay range for this position is $172,000 - $244,000 annually. The base pay range may take into account the candidate's geographic region, which will adjust the pay depending on the specific work location. The base pay offered will take into account the candidate's geographic region, job-related knowledge, skills, experience and internal equity, among other factors. In addition to the base salary, as part of our Total Rewards program, Exelixis offers comprehensive employee benefits package, including a 401k plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Employees are also eligible for a discretionary annual bonus program, or if field sales staff, a sales-based incentive plan. Exelixis also offers employees the opportunity to purchase company stock, and receive long-term incentives, 15 accrued vacation days in their first year, 17 paid holidays including a company-wide winter shutdown in December, and up to 10 sick days throughout the calendar year.

If you have a disability and need an accommodation in relation to the application and/or recruitment process, please email us at: [e-mail].

DISCLAIMER

The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.

WE ARE AN EQUAL OPPORTUNITY EMPLOYER

We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.