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Sr. Director Head of Plant Manufacturing - Vacaville (2 positions) Diversity & Inclusion

Company: Genentech
Location: Vacaville
Posted on: September 12, 2020

Job Description:

Sr. Director Head of Plant Manufacturing - Vacaville (2 positions) Vacaville

California, United States of America

Pharma Global Technical Operations (PT) is the organization that manufactures and delivers Roche’s groundbreaking therapies to 127 million patients around the world. PT is involved in producing every Roche medicine – from the development process through clinical trials – and continuing to product maturity. Our organization coordinates all aspects of production of Roche medicines in all disease areas and dosage forms at 15 plants and 11 sites around the world.

Are you passionate about leading a site manufacturing team and looking for a meaningful role? Are you a leader who can build and share an inspiring vision, who can coach leaders and teams to be better, who is a catalyst for change and world class performance, and who knows how to create the architecture that enables their network to be the best in the industry?

This position offers a unique and exciting opportunity for a senior executive to enable, coach, lead and inspire people. The Vacaville site is one of the world's largest biotechnology manufacturing plants for the large-scale production of proteins from mammalian cells. There are two cell culture production facilities located on site.

Reporting to the Vacaville Site Head General Manager, you will be a member of the Vacaville leadership team and be accountable for the safe, cost-effective and efficient manufacturing operations for one of our two cell culture production facilities. By leading an agile organization with a mindset and culture that engages our employees to bring our medicines and services to more patients faster, you will be able to influence how we as a company ensure long-term sustainability in manufacturing excellence. You have the ability to inspire people to do their best work and be committed to continuing our cultural evolution.

Your key duties and responsibilities will include:

Leadership:

Proactively promote a positive safety and quality culture and GMP operating principles to achievement of long term goals.

Create an environment of strong team spirit, timely and effective communications, sense of urgency, high motivation and inspire teams to achieve goals in the immediate and longer term.

Be an active and visible change agent, promoting flexible and open mindsets to new opportunities.

Establish strategic goals and objectives and maintain full strategic responsibility for the organization.

As a site leadership team member, drive collaboration within the site and across network activities, cross-functional planning, and decision making.

Build a strong pipeline of talent and robust succession plans for key positions, focussing on developing employees.

Embody lean leadership principles and methods while fostering a continuous improvement mindset.

Accountable for overall budget and financial performance of the Manufacturing organization.

Technical:

Ensure production of quality products according to Health Authority requirements, Roche PQS, incl. DMS, CAPA, QRM, TCM.

Optimize production output and labor efficiency while meeting required safety and quality levels.

Continuous improvement of manufacturing procedures and related equipment in collaboration with MSAT, Facilities & Engineering, and Quality

Participate in the development of production, productivity, and financial goals and manage operations so that all site goals are met.

Ensure cGMP compliance and inspection readiness for all reporting departments at all times. Actively support inspection activities.

Ensure the condition of all equipment, premises, and infrastructure in the manufacturing area are in good condition. Identify, and arrange any necessary repairs, maintenance work or technical or structural reworking within the framework of the respective competences in cooperation with the Facilities and Engineering, and MSAT groups.

Operate within the validated state of processes and equipment.

Ensure that staff are appropriately trained and qualified for the activities they perform.

Support the development of the production plan and ensure conformance with production schedules.

Responsible for in process control analysis and ensuring that the planned production can run without delay.

Further develop the operating procedures and equipment in accordance with the state of pharmaceutical technology, provided that a quality or production improvement can be achieved or a GMP requirement can be met.

Represent manufacturing in defining and refining validation strategy, investigations and technical transfers.

Continuously monitor deviations and define and implement sustainable measures to reduce deviations. Promotes problem identification and a culture of proactive problem prevention.

Who you are:

Servant and creative senior leader, motivated by our shared purpose, to generate value and impact beyond the sum of our individual contributions

Ability to coach a team of high performing leaders, catalyzing their performance to be better than the individual contributions

Able to build and lead diverse teams, develop talent and create a working culture that is transparent and values-driven to accelerate the personal growth of employees

Able to build trusted relationships through authenticity, accountability, and respect for others

Demonstrated global and cross-functional leadership through effective influencing, collaboration and cultural awareness both internally and externally

Demonstrated innovative, forward-thinking and strategic agility to build a vision

Solution-driven and courageous; empowering decision maker.

Bachelor’s degree, preferably in Science or Engineering, or equivalent combination of education and experience. Advanced degree preferred.

15+ years of relevant work experience in the pharmaceutical or related industry to include 6+ years of manufacturing/production experience.

8+ years of people management experience, including management of people manager or director level employees.

Expert knowledge of cGMP relevant to the pharmaceutical industry.

Expert knowledge and demonstrated capability to work across functional areas such as process development, maintenance and quality of pharmaceutical manufacturing facilities.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

#ptcareers

#LI-CA1

Who We Are A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

The next step is yours. To apply today, click on the "Apply online" button.

Genentech is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status. For more information about equal employment opportunity, visit our Genentech Careers page .

Vacaville

California, United States of America

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“ The important thing in science is not so much to obtain new facts as to discover new ways of thinking about them. ” – William Lawrence Bragg

Keywords: Genentech, Vacaville , Sr. Director Head of Plant Manufacturing - Vacaville (2 positions) Diversity & Inclusion, Other , Vacaville, California

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