vegas制药厂诚聘多位人才
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职位1:1 V" t" a+ x) J3 U# M1 ?. E8 K
Chemist /QC
/ u' ^3 c4 u/ U( YLocation: Las Vegas! b* v& G. L# ]2 w* Y3 \1 K' f
Job type:Full time/part time$ |/ m S3 E; g- x6 ^4 k
Salary: DOE: j) g4 m) z. |' d
Job Description:9 l8 s' A7 l% v( M3 Q
- The Chemist is responsible for the performance, recording and reporting of chemical tests of
' t; \* A+ q' n* s! Ufinished product, in-process, raw material, stability and validation samples of the Chemistry$ @$ y5 Y, A: u
Department.
" ]9 h: |4 T5 {) _4 u3 W7 w- Operate GC, HPLC, UV/VIS, FTIR, AA, pH, wet chemical equipment, Viscometer, scales1 C% A0 p1 K7 q' y9 U
and other laboratory instruments as required by the applied test methods., \: _; C6 d; ^% G% o# B @
- Perform and document the calibration of instruments, when required.3 l- R6 i9 S9 f; O
- Assist in the requisition and inventorying of laboratory supplies.
- r9 v/ w2 m f- Help with other tasks contributing to the overall operation of the laboratory as designated by
: `1 }7 x# z% Vthe Chemistry Department Manager and Supervisor.- Y! S6 v3 A# j" s. s
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EDUCATION and/or EXPERIENCE: Bachelor's degree (B.S.) Chemistry or related science degree from a college or university is required. Master/PhD degree is preferred.One year industrial work experience in the chemistry laboratory is preferred.
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& A! S% E1 U% m. s# A/ r职位2:
9 S+ q0 _- @" T5 _Regulatory Affairs Associate. A2 m" L3 c3 ?9 s$ {$ C
Location: Las Vegas
9 ?/ }" s# |: kJob type:Full time/part time1 k3 [ M) U8 w
Salary:DOE0 B. J. X. P% P2 H9 ^
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Job Description:
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- Managing the activities as assigned for regulatory affairs and compliance throughout the business.
- Ensuring a products quality during the production process and applicable regulations and procedures are adhered to (cGMP, ISO, FDA, FTC, etc.)
- Serves as the company's most responsible contact for any necessary interactions with regulatory authorities.
- Interact with domestic and foreign regulatory authorities in the same capacity as necessary. Interact with regulatory agencies to answer questions, plan meetings, obtain information, and otherwise facilitate regulatory interactions.
- Create and maintain SOP’s, assist in training, lead all audits, assist in the research and development of new products and the continuous improvement of current products.
- Be proactive to minimize or eliminate regulatory issues to help prevent any impact of adverse regulatory activities on the corporate reputation, market or bottom line.
- Lead all audits required from regulatory agencies, customers and prospects.
- Co-ordination with various stake holders, project teams, strategic sourcing, QA/QC, systems, supply chain, sales, equipment, facilities, project management to plan scale up activities in effective & timely manner.
- Investigates, reviews, and recommends new procedures, policies and/or technology that would improve or enhance the department’s capability to deliver service, quality, compliance and build sales.
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EDUCATION and/or EXPERIENCE:
( \9 l2 z- C9 p5 B8 m& D' ~0 XBachelor's degree (B.S.) Chemistry or related science degree from a college or university is required. Master/PhD degree is preferred. One year industrial work experience in the chemistry laboratory is preferred.5 c& d: G5 f+ A7 g T w
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