Manager, Validation & Laboratory Operations (Filtration, Pharmaceutical, GLP) in Shrewsbury, Massachusetts
Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
The Manager, Validation and Laboratory Operations for Cytiva is responsible for leading paid service customer specific technical projects. Leading a small team, remotely, you will work directly with external Biotech customers and internal commercial teams to define, implement, and complete customer specific technical projects. You will generate specific test protocols and reports to support customer requests and be assigned responsibility for intermediate to complex projects.
This position is part of the BIS-PDVS and will be fully remote.
What you will do:
1. Lead, delegate, and review projects of intermediate to complex complexity with no guidance and direction.
2. Co-Lead or Lead Technical consultation with customers (internal and external), involving validation testing plans and data review, test recommendations based on regulatory knowledge and expectations, leveraging SMEs.
3. Lead team collaboration and communication with the lab team to ensure all test requirements are in place.
4. Travel to customer sites for technical meetings and co-lead or lead customer trainings/presentations, using SMEs.
5. Establish project priorities and decide appropriate actions required to meet target dates.
6. Update management on the status of assigned projects, including completion, delays, or problems – lead development and implementation of countermeasures.
Who you are:
1. Bachelor’s, Master’s Degree, or PhD in Science or Life Science.
2. Prefer 5+ years of working experience in the biotech industry.
3. Background in Microbiology and Chemistry Validation testing with an understanding of Filter/Filtration concepts.
4. Skilled in advanced laboratory techniques and measurement methods; ability to perform complex test work; application of GLP as appropriate and familiar with GMP requirements.
5. Fluent in English (reading and writing).
Travel, Motor Vehicle Record & Physical/Environment Requirements:
1. Ability to travel – 10% travel, overnight.
2. Must have a valid driver’s license with an acceptable driving record.
At Cytiva we believe in designing a better, more sustainable workforce. This position is eligible for a remote work arrangement. Additional information about this remote work arrangement will be provided by your interview team.
The salary range for this role is $83,000 - $120,000 USD. This is the range that we believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance, and 401(k) to eligible employees.
Given the essential job duties of this position, the employee is required to be fully vaccinated against COVID-19 as a condition of employment, subject to reasonable accommodation and applicable law.
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
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