Pharmaceutical Validation Professional

Hiring By - Biostaffic


United Kingdom

Job Highlights

Not Disclosed

Entry level

Posted 4 months ago
Job details
Kindeva is a global pharmaceutical contract developer and manufacturer (CDMO) business headquartered in St. Paul, MN. Kindeva was established following 3M’s sale of substantially of all its drug delivery business to affiliates of Altaris Capital Partners.
Kindeva is navigating a period of dynamic change and growth as a result of the sale and business opportunities in its pipeline. Kindeva partners with global pharmaceutical companies to commercialize products, primarily through inhalation and transdermal delivery technologies.
We are looking for a talented Pharmaceutical Validation Professional to join our team. Much of what we do is to GxP standards. In this role you will provide vital scientific support to our R&D colleagues in Kindeva, which employs across the UK and US. The role would include technical support in our Laboratory Services Department, and other services to the R&D community.
Summary Of Position
The role entails the support in the R&D Laboratory Services organization for the management of the Laboratory Equipment. This includes ensuring that an equipment is compliant, operational, and maintained throughout its lifecycle. This can be achieved by ensuring that an equipment is qualified and calibrated, providing technical support to the end users, software administration and requalification. In addition, other support services include ensuring that the Laboratory Services department remains compliant and operational at all times by ensuring critical activities are completed promptly.
Job Responsibilities
  • Laboratory Equipment Management
    • Ensuring the equipment are operational, calibrated and compliant to GxP Standards.
    • Ensuring that the equipment are qualified (i.e., IQ, OQ and PQ) as per the regulatory requirements and in compliant with the procedures.
    • Ensure all necessary documentation e.g., creating and executing qualification protocols and reports are completed according to the timelines.
    • Undertaking routine software administrative support of the equipment
  • Supporting and working with the end users to ensure that the laboratory remains compliant, and the equipment are available as per the timelines.
Key Working Relationships
This role must maintain strong working relationships cross-functionally with business leaders, employees, and external partners across the global enterprise.
Skills & Experience
  • Min 2 years relevant work experience in a Pharmaceutical GxP environment
  • Familiarity in the use of applications such as Laboratory Information Management System (LIMS), Chromatography Data Systems (e.g., Empower) and Electronic Laboratory Notebook (ELN).
  • Familiarity with the analytical equipment such as High-Performance Liquid Chromatography, Gas Chromatography.
  • Bachelor’s degree from accredited university in analytical sciences or related field.
  • Excellent interpersonal and organizational skills to interface with internal customers, management and outside vendors.
Location: Primarily, this role is based in Loughborough, UK to support our R&D colleagues in person
What We Will Give To You
Attractive compensation package
Company pension scheme (up to 10% employer contribution)
25 days holiday per year (plus bank holidays) plus service days after 5 years
Company sick pay
Employee Assistance Program with 24/7 confidential helpline support for employee and immediate family
Life assurance of four times life cover salary
Flexible working hours
Wellness programmes
Employee recognition program
Employee development
Free on-site parking
Discount and cashback at many retailers
Cycle to work scheme
Flu vaccinations
Employee referral scheme

Benefits Offered?

  • No

Bonus Offered?

  • No

Travel Required?

  • No


  • United Kingdom


  • Entry level

Global Experience Needed?

  • No

Specialized Experience Needed?

  • No

Apply before:

  • Apr 13, 2024
Company Overview
Kindeva Drug Delivery
Kindeva Drug Delivery

Current Openings: 0

Kindeva is a global force in combination drug delivery and manufacturing. Leveraging more than 100 years of innovation, Kindeva provides unrivaled expertise at every stage of pulmonary & nasal, injectable, and transdermal therapy development and manufacturing. Whether determining ideal delivery and dosage or scaling sterile manufacturing and fill-finish operations, every solution is backed by extensive technological capabilities, deep regulatory knowledge, and state-of-the-art facilities across the U.S. and U.K. Kindeva’s proactive, informed solutions minimize risk and maximize confidence from ideation through commercialization, bringing high-quality products to patients in need, faster. For more information about our leading drug-device CDMO, please visit
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