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Senior Manufacturing Technician

Piramal Pharma Limited

Falkirk

On-site

GBP 60,000 - 80,000

Full time

30+ days ago

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Job summary

An established industry player seeks a Senior Manufacturing Technician to oversee high potency ADC/API manufacturing. This role involves ensuring compliance with cGMP procedures, training team members, and maintaining SHE standards. You will play a crucial part in product introduction and liaise with various departments to address issues. Join a dynamic team committed to delivering excellence in pharmaceutical manufacturing, where your contributions will directly impact product quality and safety. This is an exciting opportunity for those looking to advance their career in a supportive and innovative environment.

Qualifications

  • Degree in a scientific subject or equivalent GMP experience required.
  • Good working knowledge of GMP and chemical processing.

Responsibilities

  • Supervise manufacturing processes to ensure compliance with cGMP.
  • Train team members and maintain high SHE standards.

Skills

Verbal Communication
Written Communication
Teamwork
Attention to Detail
Interpersonal Awareness
Customer Awareness
Forward Thinking

Education

Degree in a scientific subject

Tools

SAP
Trackwise

Job description

Join to apply for the Senior Manufacturing Technician role at Piramal Pharma Ltd

3 days ago Be among the first 25 applicants

Key Roles & Responsibilities:
  • Supervise the manufacture defined cGMP procedures to deliver high potency ADC/API’s in support of launched products and clinical trial programme.
  • Proactive approach to suite readiness, structured monitoring, line clearance, BOM /Stock levels, sample control and SAP inventory.
  • Takes on a key role with the introduction of new products, liaising and communicating with relevant departments on highlighted issues.
  • Ensuring all team members are adequately trained and deliver training as and when required.
  • Effectively utilise and motivate manufacturing team to obtain the required schedule adherence.
  • Possess good verbal and written communication skills.
  • Ensure that all GMP documentation is completed “real time” and accurately in the aim of right first time.
  • Maintain high SHE Standards, carrying out all work in accordance with appropriate SHE systems.
  • Ensure that 5’s and housekeeping standards are adhered to, and suites are “audit” ready at all times.
  • Raise any deviations and REW’s as required. Progress any investigations, CAPA’s to completion through “Trackwise” within the stated timeframe.
  • Leads continuous progress within the suites.
  • Deputy for Shift Team in their absence.
Key Competencies:
  • Teamwork - As a team member, the ability and desire to work cooperatively with others on a team.
  • Communication - The ability to ensure that information is passed on to others who should be kept informed.
  • Building Collaborative Relationships - The ability to strengthen partnerships with others inside the organization who can provide information, assistance, and support.
  • Attention to Detail - Ensuring that one’s own and others’ work and information are complete and accurate.
  • Personnel Credibility - Demonstrated concern that one be perceived as responsible, reliable, and trustworthy.
  • Forward Thinking - The ability to anticipate the implications and consequences of situations and take appropriate action to be prepared for possible contingencies.
  • Interpersonal Awareness - The ability to notice, interpret, and anticipate others’ concerns and feelings, and to communicate this awareness empathetically to others.
  • Customer Awareness - The ability to demonstrate concern for satisfying one’s external and/or internal customers.
Qualifications
Essential Qualification:
  • Degree in a scientific subject or the equivalent GMP experience.
  • Possess good verbal and written communication skills.
Essential Experience:
  • Good chemical/bio-processing industry knowledge.
  • Good working knowledge of GMP.
  • Understand chemical unit operations and process chemical reaction hazards.
  • Possess good verbal and written communication skills.
  • Experience of working in clean rooms (desirable).
About Us

In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices.

Equal Employment Opportunity

Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics.

About The Team

Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle.

Seniority Level

Mid-Senior level

Employment Type

Full-time

Job Function

Management and Manufacturing

Industries

Pharmaceutical Manufacturing

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