Job Description

Kindeva Drug Delivery

Our Work Matters:

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make:

You will be leading a Quality Control team providing supervision, technical guidance, training and development whilst ensuring the release of Pharmaceutical raw materials, components and finished products for batch release, stability and customer complaints are in line with site procedures, adhering to EHS and GMP expectations, to meet business needs.

Key Responsibilities include, but are not limited to:

Maintain and promote a safe working environment. Ensure the team are taking responsibility for personal safety and the safety of others. Participate in and encourage pro-active safety and raising of documentation for safety incidents as required. Ensure completion of safety training 100% OTIF for self and team. Ensure team are following the 10 rules of GMP, working to appropriate laboratory systems, standards and procedures ensuring adherence to ALCOA. Ensure the team maintains Good Laboratory Housekeeping. Ensure completion of GMP training 100% OTIF for self and team. Ensure application of current regulatory standards to laboratory function and Kindeva procedures and practices. Effectively plan and organize resource for laboratory activities to meet business and regulatory needs. Champion the identification and implementation of CI activities for self and team. Participate as Lead for QC CI projects and Team Member for Site/Global CI projects. Effectively communicate throughout the business at all levels. Represent area of responsibility on multi-functional project teams and work closely with colleagues from other departments. Represent the department during regulatory and customer audits as required. Effectively performance manage the team, ensuring they adhere to company policies. Participate in the recruitment and growth of the team.

Skills & Experience:

Degree in a Science or related discipline is preferred but not essential. 3+ years of experience in pharmaceutical or manufacturing or similar industry. Experience of working in a GMP/GLP environment. Display of leadership skills Knowledge of pharmaceutical testing requirements, current testing techniques, software and testing equipment. Knowledge of current pharmaceutical guidelines and regulations. Computer literate, familiar with Microsoft Word and Excel.

Key Capabilities:

Inspire and motivate your team to achieve excellence and accountability. Lead by example with integrity, professionalism, and accuracy. Excellent interpersonal skills, both written & oral. Strong verbal communication skills, especially in cross-functional/leadership meetings. Adapt to changing priorities, timelines, and regulatory expectations without compromising on quality. Demonstrate strong analytical and decision-making skills. Use data to guide actions and continuously improve processes. Maintain a high standard of accuracy, completeness, and documentation. Champion data integrity and encourage a right first-time culture.

What we Offer:

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. Private Medical Insurance. 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.

Additional Information:

Working Hours:

37.5hrs per week

Location:

Charnwood Campus, Loughborough



All applicants must be eligible to work in the UK.



We believe our people make the difference at Kindeva, we look for skilled, passionate, and driven professionals to come and work with us to help us excel in manufacturing technologies and processes, which bring lifesaving products to patients worldwide.



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Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees--regardless of format--without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.



Kindeva is an Equal Opportunity Employer