Biochemist II
Onsite, Cayey, Cayey
- 求人ID
- R-557958
- Category
- Operations
- Location
- Cayey, プエルトリコ
チームワークとリアルな社会的インパクトを基盤とした製造のキャリアを築く
BDの製造部門では、患者さんや医療従事者が日々頼りにしている医療テクノロジーを生み出しています。最先端の設備を使った実践的な業務に携わり、厳格な品質・安全基準に従いながら、世界中のヘルスケアシステムに安定した供給を届ける重要な役割を担います。
経験豊富なオペレーターの方も、これから技術スキルを磨きたい方も、BDには充実したサポート環境、明確な期待値、そして成長の機会があります。BDは意義ある仕事に真摯に取り組むことにコミットしている企業であり、あなたはその中で働くことになります。世界最大級のメドテックカンパニーの一員として、世界のヘルスケアシステムを支える大規模な製造に携わり、ケアを必要とする現場に貢献することができます。
We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
Job Responsibilities
Tissue Culture (TC) Area
- Create, maintain, and test Master and Working Cell Banks of antibody-producing hybridomas.
- Conduct in-process testing for viability, secretion, and sterility.
- Process cell culture supernatant to remove debris and concentrate product prior to purification.
- Monitor the cell culture process using biochemical and immunological procedures.
- Formulate purified materials according to finished-goods specifications and dilution batch records.
Purification Area
- Perform incoming testing of culture media, ascites fluids, and other materials requiring evaluation using available purification techniques.
- Test and purify monoclonal antibodies from serum/ascites fluid and tissue culture supernatant using appropriate serum fractionation and/or column chromatography techniques.
- Formulate monoclonal antibody reagents according to finished-goods specifications and dilution batch records.
- Perform resin retesting and reclamation processes.
Conjugation Area
- Conjugate monoclonal antibodies from purified materials using required fluorophores, dyes, or other molecules.
- Monitor the conjugation process at various stages to maximize product yield and quality.
- Formulate conjugates according to finished-goods specifications and dilution batch records.
- Prepare maleimide and raw materials based on production plan requirements.
- Maintain chromatography systems, including column packing, cleaning, and equilibration, and report equipment issues as needed.
General Responsibilities
- Perform required in-process testing.
- Complete material movement transactions in SAP and perform inventory control activities to maintain accuracy.
- Maintain detailed production records, logs, and documentation.
- Generate quality reports, including Out of Specification (OOS) and Deviation Reports.
- Initiate and participate in investigations according to established quality procedures and approved protocols.
- Perform equipment cleaning, inspection, calibration verification, maintenance, and troubleshooting.
- Participate in the development and revision of Standard Operating Procedures (SOPs).
- Support project-related activities as required.
- Follow all safety procedures and actively participate in Environmental Health & Safety (EH&S) programs.
- Identify and report hazardous conditions or unsafe work practices.
- Maintain compliance with applicable regulatory requirements and participate in required regulatory training.
- Participate in the Daily Management System, including shift start-up meetings and reporting appropriate metrics.
- Participate in Continuous Improvement initiatives.
- Recommend improvements to enhance product/process quality and availability, reduce costs, and increase production capability.
- Maintain good housekeeping practices.
- Participate in Knowledge Transfer activities as required.
- Perform other related duties and assignments as needed.
Education & Experience
- Bachelor’s degree in a related scientific discipline, such as Chemistry, Biochemistry, Biology, Microbiology, or Engineering.
- Minimum of 1 year of experience in a laboratory, pharmaceutical, medical device, or biotechnology environment.
- An equivalent combination of relevant education and experience may be considered.
Knowledge & Skills
- Knowledge of methods used to create, maintain, and test Master and Working Cell Banks of antibody-producing hybridomas.
- Experience with laboratory equipment such as: Micropipettes and volumetric devices Microscopes Microplate readers CO₂ incubators Centrifuges Biosafety hoods Spectrophotometers
- Knowledge of monoclonal antibody purification using serum fractionation and/or column chromatography techniques.
- Basic understanding of chemicals and kinetic reactions.
- Knowledge of FPLC, HPLC, UV monitors, electrophoresis, and size-exclusion columns preferred.
- Knowledge of reagent formulation.
- Knowledge of GMP, FDA, ISO, and OSHA requirements highly desirable.
- Knowledge of SAP highly desirable.
- Working knowledge of Microsoft Office and the Windows environment.
- Strong analytical thinking, problem-solving, communication, interpersonal, planning, and organizational skills.
- Ability to follow established policies and procedures.
- Fully bilingual in English and Spanish.
- Willingness to travel to the U.S. mainland and offshore locations.
Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visithttps://bd.com/careers.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Required Skills
Optional Skills
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Primary Work Location
USA PR Cayey - Vicks Drive (BDB)Additional Locations
Work Shift
PR 700am-330pm M-F (United States of America)求められる人物像
BDの製造部門で活躍する人たちには、どのような特長があるでしょうか。以下のような方は、BDの製造部門できっと活躍できるはずです:
- チームワークを大切にする方
- 細部にまで注意を払える方
- 問題解決力のある方
- 結果志向の方
- 自発的に行動できる方
- 信頼できる方
より大きな社会的意義のある仕事に参加する準備はできていますか?
ここは、一貫性、チームワーク、品質を重視する方に向いた環境です。経験豊富なリーダーによるサポート、体系的なトレーニング、明確なプロセスが用意されており、大規模に患者ケアを向上させる製品づくりに貢献することができます。BDで34年のキャリアを持つベテラン社員が、真にインパクトを生み出す製造の仕事の中に見出される誇り、使命、そして可能性をどのように体現しているかをご覧ください。
人を中心に築かれた職場環境
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「BDの製品が人々の生活にどのような影響を与えているのかという話を聞くことが、私が自分の役割にワクワクする理由です。毎日、命の危険にさらされている方々を助けるために私たちが製品を出荷していることを知ることで、自己充足感を得ています。」
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「私たちの製品に自信を持てるのは、製品組立プロセスに直接携わり、十分な訓練を受けた思いやりのある仲間と働いてきたという私自身の経験だけではなく、どの工程にも高い品質を守るための確かな手順と優れたチームが整っていることを知っているからです。」
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「BDのカルチャーはとてもつながりが強く、支え合い、そして社員が大きな誇りを持っています。その誇りは、日々の業務の中にしっかりと表れています。」
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「マネジメントチームと私は、社内外の様々なトレーニングリソースとチャネルを積極的に活用し、包括的な人材育成システムを確立するとともに、社員ひとり一人に合わせたトレーニングと能力開発プランを提供してきました。マネジメントチームのメンバーのほとんどが社内昇進によるものであることを誇りに思っています。」
福利厚生
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競争力のある報酬
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退職金制度
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医療保険
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有給休暇
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育児休暇
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従業員支援プログラム(EAP)
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報奨・表彰制度
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