At Bristol Myers Squibb, we are inspired by a single vision transforming patients lives through science. In oncology, hematology, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.
Job Summary
The main purpose of this role is to inspect, maintain and repair all related plumbing and mechanical fixtures associated with any general, utility and process facility requirements at the Summit West GPDO buildings in a safe and compliant manner and in accordance to site cGMP policies and procedures. Role would include the operational oversite and maintenance of water purification systems, heating hot water systems, compressors, centralized vacuum systems, process gases, cryo tanks, freezers, refrigerators, process incubators and bulk gas distribution systems. Incumbent of the role will be responsible for maintaining all pressurized vessels according to local and state regulatory requirements.
Responsibilities
Working under minimal direction and guidance and be self-motivated, responsibilities shall include but not be limited to the following;
Respond to Customer requests in a professional and timely manner.
Respond and operate in accordance to cGMP policies and procedures.
Inspect, maintain, test, troubleshoot, adjust, repair and/or replace all related plumbing and mechanical fixtures i.e.,
Domestic water systems, backflow preventers, general and laboratory sanitary systems, general commercial plumbing fixtures, laboratory gas and vacuum distribution systems, water purification systems, steam and condensate systems
Valves, traps, heat exchangers
Operational oversite and maintenance of all rotating equipment including:
Chiller Plants, Air Compressors, Vacuum Systems, Water Purification Distribution Systems
Operational oversite and maintenance of all pressurized vessels in accordance with local and state regulatory requirements
Operational oversite and maintenance of environmentally controlled unit including
Refrigerators, Freezers, Incubators, Cryo Freezers
Knowledge of chiller plant operations
Perform general and preventative maintenance
Inspect and change water system filters, gaskets.
Assist in troubleshooting and emergency situations.
Complete necessary paperwork, i.e, Log Books, Work Tickets, PM Documentation in accordance with cGMP good documentation practices.
Demonstrate skill and care in the use of tools and materials used within plumbing/mechanical trades
Perform all work in accordance with established safety procedures.
Train colleagues as necessary.
Work with internal and external partners. Provide cGMP oversight of external vendors to ensure they are operating within the cGMP policies and procedures of the area
Other duties as assigned
Qualifications
Expert knowledge of plumbing and mechanical systems and codes.
Expert written and verbal communication skills.
Outstanding customer service skills.
Basic proficiency in Microsoft Word and Outlook.
Ability to solve basic technical problems.
Ability to meet schedules and timelines.
Strong interpersonal skills.
Basic skills in brazing techniques, welding and other pipe fitting techniques
Ability to read and comprehend blueprints, drawings, schematics, specifications, codes etc
Ability to adhere to Plumbing Codes.
Competencies:
Action Oriented
Meticulous
Tenacity
Decision Making
Demonstrates Character
Achieves Results
Detailed oriented
Methodical
Education and Experience:
High school diploma or GED.
Associates Degree or Technical Diploma
10 years of industrial plumbing/mechanical experience
3-5 years of GMP Facility experience
Working Conditions (US Only):
Physical/Mental Demands
* Work required in and around laboratory and regulated environments.
* Working in and around chemicals and potent compounds.
* Working in and around confined spaces.
* Ability to lift greater than 50 lbs.
* Ability to perform on elevated work platforms.
* This position requires regular medical surveillance and will require incumbent to wear a respirator or gown.
* Ability to work a minimum of a 40 hours work week.
* Ability to work on call for Emergency response, Overtime, and weekend shifts.
* Ability to work safely in an environment with hazardous, radioactive, and infectious materials and waste.
* Ability to work safely in an environment with exposure to high temperatures / pressure steam, compressed gasses, various noise levels, and high voltage energy supplies.
* Ability to sit, stand and move within workspace for extended periods.
* Occasional stooping, bending, stretching and lifting greater than 50lbs may be required.
* Ability to perform repetitive tasks including frequent hand to finger manipulations, grasping, pushing and pulling.
Environmental Conditions
* Ability to work safely in an environment with hazardous, radioactive, and infectious materials and waste.
* Ability to work safely in an environment with exposure to high temperature / pressure steam, and other fluids, compressed gasses, odors, various noise levels, moving parts, vibration, wet/slippery areas and high voltage energy supplies
* Environment may include working at heights, in cold temperatures, and/or constricted spaces
* Ability to work safely when alone, or with others.
* Ability to work within a GMP environment and properly gown according to room classifications and procedures
BMSCART
Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Summit, NJ
Celgene Corporation, a biopharmaceutical company, discovers, develops, and commercializes therapies for the treatment of cancer and inflammatory diseases worldwide. It offers REVLIMID, an oral immunomodulatory drug for multiple myeloma (MM), myelodysplastic syndromes (MDS), and mantle cell lymphoma; POMALYST/IMNOVID to treat multiple myeloma; OTEZLA, a small-molecule inhibitor of phosphodiesterase 4 for psoriatic arthritis and psoriasis; and ABRAXANE to treat breast, non-small cell lung, pancreatic, and gastric cancers.
The company’s products also include IDHIFA for the treatment of adult patients with relapsed or refractory acute myeloid leukemia (rrAML) with an isocitrate dehydrogenase-2 mutation; VIDAZA, a pyrimidine nucleoside analog for intermediate-2 and high-risk MDS, chronic myelomonocytic leukemia, and AML; THALOMID to treat patients with MM; and ISTODAX, an epigenetic modifier. Its preclinical and clinical-stage product candidates include small molecules, biologics, and cell therapies for immune-inflammatory diseases, myeloid diseases, epigenetics, protein homeostasis, and immuno-oncology.
The company has agreements with BeiGene, Ltd; Acceleron Pharma, Inc.; Agios Pharmaceuticals, Inc.; bluebird bio, Inc.; Lycera Corp.; Juno Therapeutics, Inc.; EXSCIENTIA LTD.; and IMIDomics SL, as well as immuno-oncology collaboration with Sutro Biopharma. Celgene Corporation was founded in 1980 and is headquartered in Summit, New Jersey.