Associate Director, Microbiology Laboratory Technical Services QC Job

Employer
Merck
Location
West Point, PA, US
Posted
October 12 2017
Organization Type
Pharma
Associate Director, Microbiology Laboratory Technical Services QC-QUA006335

Description

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Merck Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe.

The Associate Director must be an advocate for maintaining a safe work environment. This individual is responsible for ensuring compliance in the laboratory in accordance with cGMPs, and GLPs, international regulations and Merck guidelines, policies and procedures. Proactively partners with Laboratory Quality Assurance personnel to ensure compliance with regulations, guidelines and procedures.

Job Responsibilities include but are not limited to:

- The Associate Director gives direction and oversight to a team of Specialists providing technical support to the microbiology laboratories.
- This individual will provide program management leadership for projects aimed at elevating the compliance and performance of the laboratories.
- As the lead in this area the individual is expected to fully manage all aspects of assigned projects and run the business activities, including but not limited to: decision making, stakeholder management, issue identification and resolution, understanding of capacity and demand, participates and drives the tier process, as appropriate, and uses this forum to escalate concerns and best practices.
- Ensures that all process improvements and capital projects are timely, robust and in alignment with corporate goals.
- The individual in this role will also be responsible for providing microbiology support to the production departments that manufacture sterile vaccines.

Qualifications

Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life.

Required:

- Bachelor’s degree in life science, science discipline, engineering, or Microbiology

- Candidates with a Bachelor’s degree, a minimum or 8 years of experience in GMP Manufacturing environment, Pharmaceutical/Biological Quality, Operational, Technical or Regulatory function supporting manufacturing or testing operations or related industry experience in a laboratory, manufacturing, science related or regulated setting.

- For candidates with a Master’s degree, a minimum or 5 years of experience in GMP Manufacturing environment, Pharmaceutical/Biological Quality, Operational, Technical or Regulatory function supporting manufacturing or testing operations or related industry experience in a laboratory, manufacturing, science related or regulated setting.
Preferred Experience and Skills:

- Microbiology laboratory experience is strongly preferred
- Sterile Manufacturing experience
- Progressive and demonstrated Quality decision-making responsibility.
- Project Management, Change Execution Management and Team Leadership experience in a Quality function.
- Demonstrated interpersonal skills including flexibility, collaboration and inclusion skills and ability to work in a team environment.
- Demonstrated self-starter with capability to develop innovative solutions to challenges.
- Demonstrated facilitative leadership skills and able to lead teams to deliver results.
- Proven analytical aptitude, critical thinking skills and ability to apply key concepts.
- Strong written and verbal communication skills.
- In-depth working knowledge and application of GMPs/GLPs.
- Proven ability to manage multiple projects/tasks simultaneously.
- Previous people management experience; ability to develop staff

If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Visa sponsorship is not available for this position.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement​



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Quality Lab Related

Job Title:Assoc. Dir, Quality Control

Primary Location: NA-US-PA-West Point

Employee Status: Regular

Travel: Yes, 5 % of the Time

Number of Openings: 1

Shift (if applicable): 1st

Hazardous Materials: Laboratory chemicals, reagents and micro-organisms

Company Trade Name:Merck