Director: Microbiology for Medical Device Testing responsibilities include but are not limited to the following:
- Applies GMP/GLP in all areas of responsibility as appropriate
- Demonstrates and promotes the company vision
- Regular attendance and punctuality
- Ensure that the quality policy/program is understood implemented and maintained at all levels of the organization; identify prevent or correct any departures from the quality system
- Oversee operations in accordance with policies set forth in the company Personnel
- Manual and Leaders Guide; lead through vision and values of the company
- Develop efficient and effective operations and systems that support the strategic goals of the company
- Coach and develop individual and team to maximize performance
- Interact with clients as necessary to maintain and grow the business
- Build strategic relationships within the organization to achieve company goals
- Identify and evaluate issues and explore continuous improvement initiatives
- Perform administrative functions as needed e.g. attend meetings and share information; prepare reports job plans and performance reviews
- Stay technologically current in field; attend seminars and/or training courses;
- Schedule and complete sales calls and presentations
- Generate and qualify leads/prospects
- Track and follow up on bids
- Support preparation of major quotes and proposals
- Perform other duties as requested by President or designee
- Perform all functions in support of and in compliance with all state and federal employment regulations
- Conducts all activities in a safe and efficient manner
- Performs other duties as assigned
- Lead team schedule and train employees
- Ensure adherence to highest quality and efficiency standards in laboratory operations
- Ensure coverage and performance
- Foster morale and teamwork
Qualifications :
The ideal candidate would possess:
- Ph.D. preferred but not required
- Strong aseptic technique skills
- Experience working in an ISO Class 5 cleanroom with proper aseptic gowning
- Experience with Environmental Monitoring of cleanrooms
- Experience with endotoxin bioburden and sterility testing
- Experience with supervising a laboratory and managing daily requirements
- Experience with validation and routine monitoring of Purified Water systems
- Strong computer scientific and organizational skills
- Excellent communication (oral and written) and attention to detail
- Ability to work independently and as part of a team selfmotivation adaptability and a positive attitude
- Ability to learn new techniques perform multiple tasks simultaneously keep accurate records follow instructions and comply with company policies
- Strong leadership initiative and teambuilding skills
Basic Minimum Qualifications:
- Bachelors degree in Microbiology or Life Science or other related degree concentration or equivalent directlyrelated experience (two years of directly related industry experience is equivalent to one fulltime year of college in related major)
- 5 years experience in a regulated environment especially in the medical device industry a plus.
- Proficient in Microsoft Office Suite skills including electronic mail record keeping routine database activity word processing spreadsheets graphics etc
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information :
Working schedule will be MonFri 8:00am to 5:00pm. Candidates currently living within a commutable distance of Lancaster PA are encouraged to apply.
What we Offer:
- Excellent full time benefits including comprehensive medical coverage dental and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holiday
Eurofins USA BioPharma Services is a M/F Disabled and Veteran Equal Employment Opportunity and Affirmative Action employer.
Remote Work :
No
Employment Type :
Fulltime