Senior Manager, QC Head
Company: SUN PHARMA
Location: Billerica
Posted on: October 30, 2025
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Job Description:
Sun Pharma is the world’s fourth largest generics company with
presence in Specialty, Generics and Consumer Healthcare products.
Supported by more than 40 manufacturing facilities, we provide
high-quality medicines, trusted by healthcare professionals and
patients, to more than 100 countries across the globe. Over the
last two decades, Sun Pharma has established itself as a leading
player in the generics market in the U.S., and we are rapidly
ramping up our presence in the specialty branded market with a
focus on dermatology, ophthalmology and onco-dermatology. Job
Summary: Supervise the Quality Control Laboratory activities and
personnel, ensuring compliance is maintained with cGMP, ISO, GLPs
and company policies and procedures. Area of Responsibility:
Execute and review analytical quality control release, stability
and complaint (follow-up) testing for raw materials, in-process and
final products to ensure compliance with cGMPs, GLPs, ISO Quality
Assurance Procedures, SOPs and established deadlines Establish and
maintain a comprehensive QC training program for analytical
personnel and reinforce the training with appropriate assignment(s)
and delegation of responsibility Monitor and prepare formal
evaluations of employee performance to ensure continued compliance
Ensure safe operations in the laboratory Coordinate transfer of
methods (new/alternate, customer supplied (ILQ) or improved
methods) or technology (instruments) into the QC laboratory Train
QC analysts on new/improved instruments and test methods Identify,
procure, install and qualify required QC instrumentation and
equipment Establish and maintain laboratory programs to monitor and
evaluate systems or equipment (i.e. analytical instrument and
equipment, etc.) status, ensure efficient laboratory performance
and compliance with preventive maintenance, qualification, and
calibration schedules Establish and maintain laboratory programs to
process, monitor and evaluate the status of test (release,
complaint, or investigation) samples in the Quality Control
Laboratory to ensure efficient laboratory throughput Oversee and
allocate personnel required to ensure deadlines are met Direct and
close all QC Stage 1 OOS investigations, deviations, CAPA, and QA
investigations within established target dates Oversee and
continuous improvement of FDA compliant Quality System Manage the
team including mentoring and coaching of staff, establishing
priorities, and delivering projects within budget and on time Use a
team-oriented approach to problem resolution Other duties as
assigned Work Conditions: Office Lab Controlled area/clean room
Exposure to noise, heat, open flame and radiation in certain areas
Exposure to non-hazardous and hazardous chemicals, toxic metals
(arsenic, lead, and mercury) Cryogenic gases (LN 2) and radioactive
materials Requires access/work in chemical fume hoods Exposure
to/use of syringes and needles Experience: Minimum 6-8 years
related experience with minimum 0-2 years related experience in a
supervisory role preferred Comprehensive knowledge of wet chemical
and instrumental analysis methods, including method development and
validation Proficient verbal, written and interpersonal
communication skills Excellent supervisory skills Ability to work
with minimal supervision Strong chemistry theory skills Strong
organization skills Position requires a balance between
administrative (office) duties and laboratory work Understanding of
cGMP, GLPs and ISO requirements Computer literacy/proficiency; PC
with spreadsheet and or instrument control software Actual base
compensation may vary based on a number of factors, including but
not limited to geographical location and experience. In addition,
this position is part of the Annual Performance Bonus Plan, and may
be eligible for the Long Term Incentive Plan. Employees are
eligible to participate in Company employee benefit programs which
include medical, dental and vision coverage; life insurance;
disability insurance; 401(k) savings plan; flexible spending
accounts; and the employee assistance program. Employees also
receive various paid time off benefits, including vacation time and
sick time. The compensation and benefits described above are
subject to the terms and conditions of any governing plans,
policies, practices, agreements, or other materials or documents as
in effect from time to time, including but not limited to terms and
conditions regarding eligibility. If hired, employee will be in an
“at-will position” and the Company reserves the right to modify
base salary (as well as any other discretionary payment or
compensation program) at any time, including for reasons related to
individual performance, Company, or individual department/team
performance, and market factors. The preceding job description has
been designed to indicate the general nature and level of work
performed by employees within this classification. It is not
designed to contain or be interpreted as a comprehensive inventory
of all duties, responsibilities and qualifications required of
employees as assigned to this job. Nothing herein shall preclude
the employer from changing these duties from time to time and
assigning comparable duties or other duties commensurate with the
experience and background of the incumbent(s). We provide equal
employment opportunities for all current employees and applicants
for employment. This policy means that no one will be discriminated
against because of race, religion, creed, color, national origin,
nationality, citizenship, ancestry, sex, age, marital status,
physical or mental disability, affectional or sexual orientation,
military or veteran status, generic predisposing characteristics or
any other basis prohibited by law.
Keywords: SUN PHARMA, Billerica , Senior Manager, QC Head, Science, Research & Development , Billerica, Massachusetts
