Gilead Science

爱飞的鱼

Job Posting Title:  Senior Research Associate II, Analytical Chemistry  
9 a5 U  E5 f% z- y% A) Q" {Requisition Number:  1452  
% m  v( R1 T" z' \* e8 ], tCountry:  Canada
, |: w6 o2 w5 m/ J+ U. m
State:  Alberta

Job Location:  Alberta
7 w3 ?( u+ H/ Z9 s2 v3 ?
Functional Area:  RESEARCH
7 e0 C% V" S7 t; `
( y/ g' v8 C% o) M( b6 JPosition Type:  Regular
* g! e) O: j: Z5 n( ]
Full-Time / Part-Time:  Full-Time

/ J& d6 j; R1 |. e/ m: zShift:  Days
7 ?& a8 i0 y' `/ Y* x
Specific Responsibilities:  Successful candidate will participate in method development activities as part of a project team. Extensive hands on experience in HPLC, GC and LC/MS is required. Ability to work within cGMP regulations for daily work is essential. Some weekend and night shifts are required depending on project and shift schedule. Minimum M.Sc. and three years relavent experience required or Ph.D. with no relavent experience.  
Essential Duties and Job Functions:  Responsible for developing technical solutions for semi routine to moderately complex projects and issues related to the QC Chemistry department.
3 K5 A" h9 l8 d, ?  z, Z% n/ ]1 \Proposes, implements, and qualifies current and new pharmacopoeia methods to improve processes and/or ensure compliance with cGMP’s and other regulatory requirements.
5 _. L2 j3 Y) D$ w6 RProvides QC Chemistry technical expertise and counsel.
0 |% f6 i; b+ A- E+ jPerforms cleaning validations.
* g9 |+ }) ^' k. i6 O+ b2 T- |2 uWrites and executes protocols and reports.
. E6 M: N& k: G/ b5 F' e4 `2 DReviews data and results of testing to ensure compliance to appropriate specifications and protocols.
6 x$ p! L, G! @6 u# T- @: ZTroubleshoots instrumentation and test methods.
+ ?# S' w5 ^6 j: S* l( }Evaluates equipment for purchase and performs installations and qualifications of the new instruments.
# O1 \) U3 K% g& z: jPerforms method transfers to/from other organizations.
Assists in the training of QC staff.
May lead or coordinate QC and cross-functional projects.

Knowledge, Experience and Skills:  Must have a full working knowledge of current Good Manufacturing Practices (cGMPs), Good Laboratory Practices (GLPs), pharmacopoeia and regulatory requirements for testing and validation pertaining to the pharmaceutical industry. Working knowledge and proficiency with Microsoft Office software.
- `% o: J$ ?6 D
Typically requires a MSc degree and minimum 3 years relevant experience or PhD and 0 years relevant experience.

+ P1 c1 e. a! I% l# B/ U, nhttp://www.gilead.com/