vegas制药厂诚聘多位人才
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职位1:1 H" E0 I/ h& B. i3 y3 u
Chemist /QC" s; T" A# M" G% _4 K8 \
Location: Las Vegas# B r) Y) U# \8 ?+ P
Job type:Full time/part time
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% |3 [ Y! x D- B2 X" v5 NJob Description:* d; [# [! K) v! o( w
- The Chemist is responsible for the performance, recording and reporting of chemical tests of/ p$ u3 H" ]' n1 Y5 L( H4 Y
finished product, in-process, raw material, stability and validation samples of the Chemistry
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5 u/ [* m& S. t, p# Z- Operate GC, HPLC, UV/VIS, FTIR, AA, pH, wet chemical equipment, Viscometer, scales$ q# D3 {1 G4 ?* O5 q& `
and other laboratory instruments as required by the applied test methods.& J0 a' L/ l, F1 O! z
- Perform and document the calibration of instruments, when required.- @: Y; Q: o4 m. i7 t( d6 I
- Assist in the requisition and inventorying of laboratory supplies." `) _3 [, l4 l( o2 y. s
- Help with other tasks contributing to the overall operation of the laboratory as designated by
* d) ~6 u) I2 d- W" Tthe Chemistry Department Manager and Supervisor.
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* c" C% h j0 J' d1 ~) aEDUCATION 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.- p; V x" w- c( C8 K
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职位2:
. H/ v( j) f1 \- ]* CRegulatory Affairs Associate
7 N; F/ u9 q% G4 wLocation: Las Vegas
' Q# N+ Q7 X' I$ }+ fJob type:Full time/part time
3 [) j* J# N: C! R9 L/ S5 ]Salary:DOE5 A7 p) p3 c2 n) M. j4 a8 R: \
) t0 t: Y4 J( n; l+ g5 q# q8 QJob 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: ) y) l( M1 B8 W) h) n. c- `
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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