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Manufacturing Project Support

3 months ago

Upper Hutt, New Zealand MSD Full time

Job Description

Manufacturing Project Support - 12 month contract

  • 12-month Fixed Term Contract, Full-time position
  • With competitive renumeration, bonus and benefits
  • Location: New Zealand, Wellington - Upper Hutt
  • Upskill and growth in an area you’re passionate about, whilst being fully supported and encouraged
  • Join a trusted Global leading Animal Health organisation and be part of a dedicated and welcoming team

This position will perform manufacturing tasks assigned from capital projects. You will also be required to act as an interface between Manufacturing, Quality, Validation, Engineering and Projects, utilising experience and knowledge from manufacturing to assist in project execution.

You will also have the responsibility for authoring, reviewing and executing manufacturing, validation and project documentation and protocols.

What You Will Do

Responsibilities include, however not limited to:

Complete required documentation to agreed timelines:

  • Change control
  • Author and/or review URS, IQ/OQ/PQ/PV documents
  • Review and contribute to PFDs, P&IDs and Sequence Sheets
  • Complete new equipment introduction forms and assessments
  • Manage update of manufacturing procedures, batch records and logbooks for updated processes and new equipment
  • Communicating clearly and in a timely way with other members of the Manufacturing Team and other departments to ensure the smooth flow of documentation allowing adequate time for review and approval

Ensure compliance with regulatory and company requirements by:

  • Completing all GMP documentation in accordance with GDP
  • Ensuring project areas maintain high housekeeping standards
  • Completing assigned CAPA in required timeframes

Contribute Manufacturing experience to Projects

  • Participate and complete assigned actions to ensure achievement of the project outputs
  • Schedule daily activities with project engineers to ensure project milestones are achieved
  • Report progress and potential issues to management
  • Recommend solutions/options to potential issues to management and project team
  • Use process and product knowledge to ensure project outcome is fit for the process and business
  • Liaise with other SMEs to fill specific knowledge gaps
  • Maintain excellent communication across all stakeholder groups
  • Execute validation protocols

Ensure the highest possible safety standards are met by:

  • Carrying out task observations
  • Taking responsibility for own and others safety
  • Ensure Safe by Choice culture is promoted to achieve Target Zero
  • Ensuring hazards are identified across projects

During your 12 months contract you will be required to be an active member of the Manufacturing team by:

  • Attending manufacturing meetings
  • Providing on-the-job training for other members of the Manufacturing team
  • Providing feedback and updates to Production manager and wider team
  • Maintaining competence in relevant manufacturing procedures
  • Providing occasional technical expertise to problem solving and deviation investigation

What You Must have

  • Science degree or equivalent preferred
  • Two years manufacturing experience in a vaccine or pharmaceutical environment.
  • Experience with GMP
  • Project experience
  • Validation experience
  • Computer Skills: Spreadsheet, Word

What You Can Expect

  • Exposure to upskill and develop in your role
  • Flexibility and opening doors to other opportunities and skillsets
  • Joining a collaborative team of likeminded individuals

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

Current Employees apply HERE

Current Contingent Workers apply HERE

Secondary Language(s) Job Description:

Science degree or equivalent preferred

Two years manufacturing experience in a vaccine or pharmaceutical environment.

Experience with GMP

Certified trainer

Production equipment operation and Validation experience

Computer Skills: Spreadsheet, Word, SAP

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, 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:

Project Temps (Fixed Term)

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

08/30/2024

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Job Posting End Date:08/30/2024


A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Requisition ID:R305354