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Quick apply
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Implementation Associate information
See Oxnard, CA salary details
$47.1K - $61.2K
8% of jobs
$61.2K - $75.3K
16% of jobs
$76.3K is the 25th percentile. Wages below this are outliers.
$75.3K - $89.4K
12% of jobs
$89.4K - $103.5K
12% of jobs
The median wage is $106.7K / yr.
$103.5K - $117.6K
12% of jobs
$117.6K - $131.7K
6% of jobs
$131.7K - $145.9K
7% of jobs
$149K is the 75th percentile. Wages above this are outliers.
$145.9K - $160K
11% of jobs
$160K - $174.1K
8% of jobs
$174.1K - $188.2K
5% of jobs
$188.2K - $202.3K
3% of jobs
$47.1K
$119.6K
$202.3K
How much do implementation associate jobs pay per year?
What are the key skills and qualifications needed to thrive as an Implementation Associate, and why are they important?
What are Implementation Associates?
What are some common challenges Implementation Associates face when managing multiple client projects simultaneously?
What is the difference between Implementation Associate vs Project Coordinator?
| Aspect | Implementation Associate | Project Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, relevant certifications (e.g., PMP, Six Sigma) | Bachelor's degree, often certifications in project management |
| Work Environment | Client-facing, technical, consulting or software deployment settings | Office-based, administrative, and planning environments |
| Employer & Industry Usage | Tech, healthcare, consulting firms | Corporate, non-profit, government sectors |
| Common Search & Comparison | Implementation Associate vs Project Coordinator |
The Implementation Associate typically focuses on deploying solutions, coordinating technical tasks, and working closely with clients during project rollouts. In contrast, the Project Coordinator manages project schedules, resources, and communication across teams. While both roles require strong organizational skills and some project management knowledge, Implementation Associates often have a more technical or client-facing focus, whereas Project Coordinators handle broader project logistics and administration.

Other
Posted 6 days ago
Job description
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: ATO Quality Control Chemistry and Biochemistry
Duration: 1+ years (with likely extensions)
Notes: Onsite. Entry-level
Posting Date: 2/18/22
3 Key Consulting is hiring a Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Under general supervision, this position will perform routine procedures and testing in support of the Quality Control Chemistry group. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Routine analytical testing - Documenting, computing, compiling, interpreting and entering data - Maintaining and operating specialized equipment - Initiating and / or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks.
Why is the Position Open?
Supplement additional workload on team.
Top Must-Have Skill Sets:
- Must have bachelor's degree & 1-3 years of industry experience, open to the industry - manufacturing, cosmetics, pharma, biotech etc.
- Must have cGMP Experience & Experience in general compendia testing
- Flexible hours
Day to Day Responsibilities:
- Routine analytical testing.
- Documenting, computing, compiling, interpreting and entering data.
- Maintaining and operating specialized equipment.
- Initiating and / or implementing changes in controlled documents.
- Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks.
- General Lab housekeeping
Basic Qualifications:
- Must have bachelor's degree & 1-3 years of industry experience, open to the industry - manufacturing, cosmetics, pharma, biotech etc.
- Must have cGMP Experience & Experience in general compendia testing.
Red Flags:
- Travel Distance
- Lack of flexibility
Interview process:
Phone screening followed by in-person interview.
We invite qualified candidates to sendyour resume toresumes@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.
About 3 Key Consulting
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
1 - 10 Employees
Headquarters location
Simi Valley, CA, US
Year founded
2009