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Merck Associate Director, Bio Technology Solutions Lead in Elkhorn, Nebraska

Job Description

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates, and finished products.

Goal

  • Managing the Bio Technology Solutions (BTS) activities at the Elkhorn, Nebraska site within Global Animal Health Manufacturing (GAHM)

  • Works together with Site Leadership Team to achieve our company's GAHM business goals

  • Direct reports 3-8 individual contributors

  • Management and the control of the portfolio of Antigen and Vaccine related technical projects within the AH site

  • Provide guidance and direction to the teams to enable reliable supply and new products commercialization

  • Partner with the relevant organization within Elkhorn Site to define the right priorities for the different projects

Primary Responsibilities

  • Responsible for the management and the control of the portfolio of BTS related technical projects within the Elkhorn site.

  • Final responsibility for the execution of these LM related technical projects lies with the incumbent.

  • Interface primarily with the Elkhorn Plant Site Manager and its Leadership Team

  • Clearly define the requested services,

  • Follow up the quality and the timeliness of the delivered services,

  • Evaluate the future needs and services for upcoming projects on mid-long and long term.

  • Participate on teams in problem solving activities using Lean Manufacturing tool to ensure direction and control of continuous improvement, waste reduction and yield improvement.

  • Activities and Projects to be managed:

  • Provide technology support to production

  • Guidance to the local teams to align on strategic priorities and local priorities

  • Gathers voice of customer and voice of business, challenges and converts into action

  • Transfer (implement) technologies to agreed schedules, milestones and objectives, and cost

  • Process robustness improvements to increase revenue (e.g. yield improvements, improved line utilization)

  • Supports investment requests/processes and is responsible for the Biotechnological input

  • Providing support and enables connection to other Bio Technology Solutions teams globally

  • Support Regulatory Affairs to review Manufacturing Outline (Drug Master File/Master Manufacturing Instructions) and GCMs (Global Change Management)

  • Manage own competing timelines and prioritize critical tasks

  • Ensure compliance with corporate and regulatory requirements

  • The incumbent is responsible for workforce planning and talent development for the Elkhorn BTS team, taking into consideration technical gaps and needs for the future

  • Assure area activities comply with our Company policies, EHS, governmental regulations, etc. and that all expectations are clearly defined and communicated

Education Minimum Requirements

  • Bachelor degree with minimum eight (8) years of experience in manufacturing within the health care industry

  • Preferred: Master degree with a minimum six (6) years of experience in manufacturing within the health care industry OR a PhD with a minimum three (3) years’ experience in manufacturing within the health care industry

Required Experience and Skills

  • Vaccine/large molecule development or manufacturing

  • Leadership role/supervisory role

  • Proven track record of managing project portfolios

  • Proven track record of talent development

  • Leading and influencing cross functional teams

  • Strategic and effective analytical and problem-solving skills

  • Understanding Regulatory/Compliance requirements

  • Demonstrated ability to communicate effectively with multiple teams and levels within the organization

Our Manufacturing & Supply Division is dedicated to being the most trusted supplier of bio-pharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create a reliable global manufacturing network that’s devoted to delivering a high quality, reliable supply to customers and patients on time, every time.

Who we are …

We are known as Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.

What we look for …

In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth .

INVENT.

IMPACT.

INSPIRE.

NOTICE FOR INTERNAL APPLICANTS

In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.

If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor.

US and Puerto Rico Residents Only:

If you need an accommodation for the application process please email us at [email protected]

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

EEOC Poster at https://www.dol.gov/sites/dolgov/files/ofccp/regs/compliance/posters/pdf/eeopost.pdf

EEOC GINA Supplement​ at https://www.eeoc.gov/sites/default/files/migratedfiles/employers/eeocgina_supplement.pdf

OFCCP EEO Supplement at https://www.dol.gov/ofccp/regs/compliance/posters/pdf/OFCCPEEOSupplementFinalJRFQA508c.pdf

OFCCP Pay Transparency Rule at https://www.dol.gov/ofccp/pdf/pay-transp%20EnglishformattedESQA508c.pdf

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

Search Firm Representatives Please Read Carefully

Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

Domestic/International

VISA Sponsorship:

Yes

Travel Requirements:

10%

Flexible Work Arrangements:

Flex Time, Job Sharing, Telecommuting, Work Week

Shift:

1st - Day

Valid Driving License:

Yes

Hazardous Material(s):

n/a

Number of Openings:

1

Requisition ID: R79596

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